Sustained release formulation of interleukin-10 for wound treatment and related methods

ABSTRACT

A sustained release formulation of interleukin-10 for wound treatment and related methods is provided.

STATEMENT REGARDING FEDERALLY SPONSORED R&D

This invention was made with government support under GM098831 awardedby the National Institutes of Health. The government has certain rightsin the invention.

INCORPORATION BY REFERENCE TO ANY PRIORITY APPLICATIONS

Any and all priority claims identified in the Application Data Sheet, orany correction thereto, are hereby incorporated by reference under 37CFR 1.57.

BACKGROUND

1. Field

This disclosure is directed to a sustained release formulation ofinterleukin-10 (IL-10) for wound treatment and related methods.

2. Description of the Related Technology

Each year, 100 million patients acquire scars, some of which causeconsiderable morbidity, including loss of physical function, reducedtissue integrity and in some disease states a predisposition torepetitive injury.

Scarring is the normal process by which postnatal mammals heal wounds.It is initiated by an inflammatory response followed by fibroblastmediated deposition of collagen with subsequent remodeling. Scars arecharacterized by haphazard collagen deposition, a flattened epidermisand a dropout of dermal appendages. These scars can have significantfunctional and psychosocial sequelae. Currently, there is a significantunmet market need for an effective skin regenerating, anti-scarringagent.

Prenatal mammals heal dermal wounds without scar and is characterized byan attenuated inflammatory response. Reverting the wound environment ofthe postnatal scarring phenotype to a more “fetal-type” milieu toachieve scarless tissue repair is of interest.

In view of the limitation of present treatments, there exists a desirefor development of new methods and products useful for treating wounds.

SUMMARY

Some embodiments provide methods for treating wounds with sustainedrelease formulations of interleukin-10.

Some embodiments provide methods for preventing or reducing scarring orfibrosis with sustained release formulations of interleukin-10.

Some embodiments provide an extended release biocompatible compositionfor preventing or reducing scarring of an incision or wound site in asubject, comprising: a biodegradable support scaffold; and IL-10,wherein the amount of IL-10 in the composition is from about 0.2 μM toabout 2.5 μM.

Some embodiments provide an extended release biocompatible compositionfor preventing or reducing scarring of an incision or wound site in asubject, comprising: a biodegradable support scaffold; and IL-10,wherein the biodegradable support scaffold is configured to release fromabout 0.015 nM to about 0.015 μM of IL-10 over a period of time at theincision or wound site.

Some embodiments provide a method for preventing or reducing scarring orprocess characterized by fibroplasia including but not limited to postsurgical wounds, traumatic wounds, keloids, hypertrophic scars, burncontractures, solid organ fibrosis, and intraabdominal adhesions byadministering a therapeutically effective amount of IL-10 to a locationin a subject for a period of time sufficient to prevent or reducescarring or fibrosis, said administering comprising a singleadministration of a composition as disclosed and described herein to anincision or wound site in the subject. Some such embodiments provide amethod for preventing or reducing scarring or process characterized byexcessive fibroplasia including but not limited to pathologic scars andkeloids.

Some embodiments provide a method for preventing or reducing scarring orprocess characterized by fibroplasia by administering a therapeuticallyeffective amount of IL-10 to a location in a subject for a period oftime sufficient to prevent or reduce scarring or fibrosis, saidadministering comprising administration of the as disclosed anddescribed herein to a site at risk for fibroplasia in the subject. Somesuch embodiments provide a method for preventing or reducing scarring orprocess characterized by excessive fibroplasia including but not limitedto pathologic scars and keloids.

Some embodiments provide a method for preventing or reducing scarring ofan incision or wound comprising administering a therapeuticallyeffective amount of IL-10 to a location in a subject for a period oftime sufficient to prevent or reduce scarring, said administeringcomprising a single administration of the composition of any one of thepreceding claims to an incision or wound site in the subject.

Some embodiments provide method for preventing or reducing scarring ofan incision or wound in a subject, comprising: providing the compositionas disclosed and described herein; and introducing the composition to alocation by administration of the composition; and maintaining an amountof IL-10 for a period of time sufficient to prevent or reduce scarringat the location.

Some embodiments provide a method for preventing or reducing scarring ofan incision or wound in a subject, comprising: providing a compositionas disclosed and described herein; and introducing the composition to alocation in a single administration; and maintaining an amount of IL-10for a period of time sufficient to prevent or reduce scarring at thelocation.

Some embodiments provide a method for preventing or reducing scarring ofan incision or wound comprising administering a therapeuticallyeffective amount of IL-10 to a location in a subject for a period oftime sufficient to prevent or reduce scarring, said administeringcomprising administration of the composition as disclosed and describedherein to an incision or wound site in the subject.

In some embodiments, the type of wound to be treated with the extendedrelease biocompatible composition can be a penetrating type wound, suchas, for example, a puncture, laceration, or bullet or shrapnel wound. Insome embodiments, the type of wound to be treated with the extendedrelease biocompatible composition can be a non-penetrating type wound,such as, for example, grazes, abrasions, skin grafts, or burns.

In some embodiments, the type of wound to be treated with the extendedrelease biocompatible composition can be a laceration or other open typewound. For example, an individual or medical aid personnel can treat thewound by utilizing a system comprising a topically-applied source of anextended release biocompatible composition and a surgical dressing.

Some embodiments provide a kit comprising: an extended releasebiocompatible composition and a dressing. In some aspects, the dressingcan be a surgical dressing. In some aspects, the dressing can be a fielddressing.

Some embodiments provide a method of evaluating a composition fortreating a wound including: providing a dosage of the composition to awound in a statistically relevant number of animals; and evaluating thewound in each animal after a period of time using an Assessment Scalevalue to obtain an Assessment Scale score, wherein said Assessment Scalescore is based on the measurement of at least 2 parameters selected fromthe group consisting of i) the quantification of topography, ii)epidermal height, and iii) the nuclear orientation of the basalkeratinocytes in the epidermis; and iv) the quantification of the scararea, v) dermal appendages, and vi) vascularity (vessel density) in thedermis of the scars. In some embodiments, each parameter is calculatedto provide an Assessment Scale value (INDEX), wherein an AssessmentScale score is calculated by (^(n)Σ INDEX/n)×100 where n is the numberof parameters being evaluated.

It is provided that, in some embodiments, when IL-10 is discussed in thespecification and claims that the IL-10 related peptides disclosed inUS. Publication No. 20080139478 or a fragment or partially modified formof IL-10 disclosed in U.S. Pat. No. 7,052,684, the relevant disclosuresof which are incorporated herein in their entireties, may be included inplace of IL-10 in the compositions or methods as disclosed and describedherein.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1(A) and (B) depict in vitro and in vivo properties of sustainedrelease of rIL-10.

FIG. 2(A)-(F) depict scar suppression and wound healing by sustainedrelease of IL-10.

FIG. 3(A)-(E) compares epidermal and dermal parameters for treatingwounds with gel only (control), Composition 2 (HH-10) and lentiviralover expression of IL-10 (LV IL-10).

DETAILED DESCRIPTION

This disclosure relates to treating wounds and preventing or reducingfibrosis with an extended release biocompatible composition suitable fordirectly introducing into a wound and/or as a topical application.

As used herein the term “wounds” refers to any condition which mayresult in fibrosis. In particular, this includes fibrosis resulting froman injury or surgery.

As used herein the term “fibrosis” refers to the formation of excessfibrous connective tissue in an organ or tissue in a reparative orreactive process. This can be a reactive, benign, or pathological state.In response to injury this is called scarring and if fibrosis arisesfrom a single cell line this is called a fibroma. Physiologically thisacts to deposit connective tissue, which can obliterate the architectureand function of the underlying organ or tissue. Fibrosis can be used todescribe the pathological state of excess deposition of fibrous tissue,as well as the process of connective tissue deposition in healing.Examples of fibrosis include, but are not limited to, pulmonaryfibrosis, glomerulonephritis, cirrhosis of the liver, systemicsclerosis, scleroderma, proliferative vitreoretinopathy, and scar tissueformed as a result of injury, surgery, or burn.

While not bound by any theory, it is believed that the beneficialeffects of the recited compositions may be achieved through biologicalactivity of Interleukin-10 (IL-10) inhibiting inflammation at a woundsite.

IL-10 was identified as a product of Th2 cells (Fiorentino, D. F. andModdman, T. R., 1989, J. Exp. Med., 170: 2081 2095) and identified as aproduct of B-cell lymphomas that prolonged the survival of mast cellsand enhanced proliferation of thymocytes (O'Garra, A. et al., 1990,Internal Immunol., 2: 821 823).

Molecular characterization of human and murine IL-10 by Moore, K. W. etal. (1990, Science, 248: 1230 1234) and Vieira, P. et al. (1991, Proc.Natl. Acad. Sci. USA, 88: 1172 1176) showed that there was an 80%homology of their nucleotide sequences. Mouse IL-10 (mIL-10) proteinconsists of 157 amino acids with two potential N-glycosylation sitesalthough glycosylation is not essential for the biological activities ofmIL-10. Human IL-10 (hIL-10) protein consists of 160 amino acids withone potential N-glycosylation site which is not used (Vieira et al.,1991). Both mIL-10 and hIL-10 contain four cysteine residues that formtwo intramolecular disulphide bonds generating biologically activehomodimers with molecular weights of 32 kDa and 39 kDa respectively.Although there is 80% homology between hIL-10 and mIL-10, only hIL-10acts on both human and mouse cells, whereas mIL-10 has speciesspecificity activity (Vieira et al., 1991; Kim, J. M. et al., 1992, J.Immunol., 148: 3618 3623).

There are many cellular sources and major biological activities ofIL-10, all of which may play some role in the wound microenvironment. Ithas been shown that IL-10 possesses many stimulatory and inhibitoryeffects. For example, van Vlasselar et al. (1994, J. Cell Biol., 124:569 577) showed that IL-10 inhibited TGF-β synthesis required forosteogenic commitment of mouse bone marrow cells, and hence theresulting mineralized matrix, whereas Go et al (1990, J. Exp. Med., 172:1625 1631) showed IL-10 to be a novel B-cell stimulatory factor. IL-10has also been shown by Bogdan et al. (1991, J. Exp. Med., 174: 15491555) to directly act on macrophages and inhibit their subsequentactivation and hence release of pro-inflammatory cytokines (see alsoBerg. D. J. et al., 1995, J. Exp. Med., 182: 99 10; Chemoff, A. E. etal., 1995, J. Immunol. 154 (10): 5492 5499).

Some embodiments relate to a method for treating a wound. In someembodiments, the wound is a postsurgical wound. In some embodiments, thewound is a trauma wound. In some embodiments, the method of treating thewound can comprise: introducing an extended release biocompatiblecomposition into the wound.

Some embodiments provide an extended release biocompatible compositionfor preventing or reducing scarring of an incision or wound site in asubject, comprising: a biodegradable support scaffold; and IL-10,wherein the amount of IL-10 in the composition is from about 0.2 μM toabout 2.5 μM.

Some embodiments provide an extended release biocompatible compositionfor preventing or reducing scarring of an incision or wound site in asubject, comprising: a biodegradable support scaffold; and IL-10,wherein the amount of IL-10 in the composition is from about 0.2 μM toabout 2.5 μM.

In some embodiments, the extended release biocompatible compositioncomprises an amount of biodegradable support scaffold from about 10% toabout 59% based on the total amount of the extended releasebiocompatible composition. In some embodiments, the extended releasebiocompatible composition comprises an amount of biodegradable supportscaffold from about 15% to about 85% based on the total amount of theextended release biocompatible composition. In some embodiments, theextended release biocompatible composition comprises an amount ofbiodegradable support scaffold from about 20% to about 80% based on thetotal amount of the extended release biocompatible composition. In someembodiments, the extended release biocompatible composition comprises anamount of biodegradable support scaffold based on the total amount ofthe extended release biocompatible composition of about 10%, 15%, 20%,25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85% or 90%or a range defined by any two of the preceding values.

In some embodiments, the biodegradable support scaffold compriseshyaluronan or a hyaluronan moiety. In some embodiments, the hyaluronanis hyaluronic acid. In some embodiments, the biodegradable supportscaffold comprises an amount of hyaluronan or a hyaluronan moiety fromabout 10% to about 90% based on the total amount of the biodegradablesupport scaffold. In some embodiments, the biodegradable supportscaffold comprises an amount of hyaluronan or a hyaluronan moiety fromabout 10% to about 90% based on the total amount of the biodegradablesupport scaffold. In some embodiments, the biodegradable supportscaffold comprises an amount of hyaluronan or a hyaluronan moiety fromabout 30% to about 70% based on the total amount of the biodegradablesupport scaffold. In some embodiments, the biodegradable supportscaffold comprises an amount of hyaluronan or a hyaluronan moiety fromabout 40% to about 60% based on the total amount of the biodegradablesupport scaffold. In some embodiments, the biodegradable supportscaffold comprises an amount of hyaluronan or a hyaluronan moiety basedon the total amount of the biodegradable support scaffold of about 10%,15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%,85% or 90% or a range defined by any two of the preceding values.

In some embodiments, the biodegradable support scaffold comprises aheparin or heparan sulfate. In some embodiments, the biodegradablesupport scaffold comprises an amount of heparin or heparan sulfate fromabout 10% to about 90% based on the total amount of the biodegradablesupport scaffold. In some embodiments, the biodegradable supportscaffold comprises an amount of heparin or heparan sulfate from about10% to about 90% based on the total amount of the biodegradable supportscaffold. In some embodiments, the biodegradable support scaffoldcomprises an amount of heparin or heparan sulfate from about 30% toabout 70% based on the total amount of the biodegradable supportscaffold. In some embodiments, the biodegradable support scaffoldcomprises an amount of heparin or heparan sulfate from about 40% toabout 60% based on the total amount of the biodegradable supportscaffold. In some embodiments, the biodegradable support scaffoldcomprises an amount of heparin or heparan sulfate moiety based on thetotal amount of the biodegradable support scaffold of about 10%, 15%,20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85% or90% or a range defined by any two of the preceding values.

In some embodiments, the biodegradable support scaffold comprisescollagen. In some embodiments, the collagen is human collagen. In someembodiments, the collagen is Type-I collagen. In some embodiments, thecollagen is Type-III collagen. In some embodiments, the collagen isType-I collagen, Type-II collagen or Type-III collagen, or anycombination thereof. In some embodiments, the biodegradable supportscaffold comprises an amount of collagen from about 10% to about 90%based on the total amount of the biodegradable support scaffold. In someembodiments, the biodegradable support scaffold comprises an amount ofcollagen from about 10% to about 50% based on the total amount of thebiodegradable support scaffold. In some embodiments, the biodegradablesupport scaffold comprises an amount of collagen from about 15% to about40% based on the total amount of the biodegradable support scaffold. Insome embodiments, the biodegradable support scaffold comprises an amountof collagen from about 20% to about 30% based on the total amount of thebiodegradable support scaffold. In some embodiments, the biodegradablesupport scaffold comprises an amount of collagen based on the totalamount of the biodegradable support scaffold of about 10%, 15%, 20%,25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85% or 90%or a range defined by any two of the preceding values.

In some embodiments, the biodegradable support scaffold comprisespolyethylene glycol (PEG) or a PEG moiety. In some embodiments, thebiodegradable support scaffold comprises an amount of PEG or a PEGmoiety from about 10% to about 90% based on the total amount of thebiodegradable support scaffold. In some embodiments, the biodegradablesupport scaffold comprises an amount of PEG or a PEG moiety from about10% to about 50% based on the total amount of the biodegradable supportscaffold. In some embodiments, the biodegradable support scaffoldcomprises an amount of PEG or a PEG moiety from about 15% to about 40%based on the total amount of the biodegradable support scaffold. In someembodiments, the biodegradable support scaffold comprises an amount ofPEG or a PEG moiety from about 20% to about 30% based on the totalamount of the biodegradable support scaffold. In some embodiments, thebiodegradable support scaffold comprises an amount of PEG or a PEGmoiety based on the total amount of the biodegradable support scaffoldof about 0.1%, 0.5%, 1%, 2%, 3%, 4%, 5%, 10%, 15%, 20%, 25%, 30%, 35%,40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85% or 90% or a rangedefined by any two of the preceding values.

In some embodiments, the biodegradable support scaffold comprisesdisulfide linkages.

In some embodiments, the biodegradable support scaffold comprises across-linker. In some embodiments, the biodegradable support scaffoldcomprises an amount of cross-linker from about 10% to about 50% based onthe total amount of the biodegradable support scaffold. In someembodiments, the biodegradable support scaffold comprises an amount ofcross-linker from about 15% to about 40% based on the total amount ofthe biodegradable support scaffold. In some embodiments, thebiodegradable support scaffold comprises an amount of cross-linker fromabout 20% to about 30% based on the total amount of the biodegradablesupport scaffold. In some embodiments, the biodegradable supportscaffold comprises an amount of cross-linker based on the total amountof the biodegradable support scaffold of about 10%, 15%, 20%, 25%, 30%,35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85% or 90% or a rangedefined by any two of the preceding values. In some embodiments, thecross-linker comprises a PEG moiety.

In some embodiments, a site that is at risk of fibroplasia orcharacterized by fibroplasia is a site that, upon incision, wounding orother injury, would incur scarring or fibrosis if not treated by thecompositions and/or methods provided herein. For example, in someembodiments, a site that is at risk of fibroplasia or characterized byfibroplasia does not include a site that has been pre-treated by IL-10or other wound healing composition prior to incision, wounding or otherinjury. While not intending to be bound by the following, it iscontemplated that the wound healing process of a site that has beenpre-treated by IL-10 or other wound healing composition prior toincision, wounding or other injury, is not the same as the wound healingprocess when a composition is administered only subsequent to theincision, wounding or other injury. And the present methods andcompositions are designed to provide a manner for wound healing thatdoes not require pre-treatment by IL-10 or other wound healingcomposition prior to incision, wounding or other injury. Someembodiments provide a method for preventing or reducing scarring orprocess characterized by fibroplasia including but not limited topostsurgical wounds, traumatic wounds, hypertrophic scars, burncontractures, solid organ fibrosis, and intraabdominal adhesions byadministering a therapeutically effective amount of IL-10 to a locationin a subject for a period of time sufficient to prevent or reducescarring or fibrosis, said administering comprising a singleadministration of a composition as disclosed and described herein to anincision or wound site in the subject. Some such embodiments provide amethod for preventing or reducing scarring or process characterized byexcessive fibroplasia including but not limited to pathologic scars andkeloids.

Some embodiments provide a method for preventing or reducing scarring ofan incision or wound comprising administering a therapeuticallyeffective amount of IL-10 to a location in a subject for a period oftime sufficient to prevent or reduce scarring, said administeringcomprising a single administration of the composition as disclosed anddescribed herein to an incision or wound site in the subject.

Some embodiments provide a method for preventing or reducing scarring ofan incision or wound in a subject, comprising: providing a compositionas disclosed and described herein; and introducing the composition to alocation in a single administration; and maintaining an amount of IL-10for a period of time sufficient to prevent or reduce scarring at thelocation.

In some embodiments, the period of time is at least about 1 day. In someembodiments, the period of time is at least about 2 days. In someembodiments, the period of time is at least about 3 days. In someembodiments, the period of time is at least about 4 days. In someembodiments, the period of time is about 2 to about 30 days. In someembodiments, the period of time is about 3 to about 7 days. In someembodiments, the period of time is at least about 1, 2, 3, 5, 7, 10, 12,15, 18, 20 or 30 days or a range defined by any two of the precedingvalues.

Some embodiments provide an extended release biocompatible compositionfor preventing or reducing scarring in a subject, comprising: abiodegradable support scaffold; and IL-10, wherein the biodegradablesupport scaffold is configured to release from about 0.015 nM to about0.015 μM of IL-10 over a period of time to the dermis, epidermis, woundmicroenvironment, wound tissue homogenate, serum, plasma, or otherrelevant anatomical site for increased fibrosis.

In some embodiments, the amount of IL-10 in the dermis, epidermis, woundmicroenvironment, wound tissue homogenate, serum, plasma, or otherrelevant anatomical site for increased fibrosis is about 0.015 nM, 0.020nM, 0.025 nM, 0.030 nM, 0.035 nM, 0.040 nM, 0.045 nM, 0.050 nM, 0.055nM, 0.060 nM, 0.065 nM, 0.070 nM, 0.075 nM, 0.080 nM, 0.085 nM, 0.090nM, 0.095 nM, 0.100 nM, 0.110 nM, 0.120 nM, 0.130 nM, 0.140 nM, 0.150nM, 0.160 nM, 0.170 nM, 0.180 nM, 0.190 nM, 0.200 nM, 0.220 nM, 0.240nM, 0.260 nM, 0.280 nM, 0.300 nM, 0.350 nM, 0.400 nM, 0.450 nM, 0.500nM, 0.550 nM, 0.600 nM, 0.650 nM, 0.700 nM, 0.750 nM, 0.800 nM, 0.850nM, 0.900 nM, 0.950 nM, 1.00 nM, 1.10 nM, 1.20 nM, 1.30 nM, 1.40 nM,1.50 nM, 1.60 nM, 1.70 nM, 1.80 nM, 1.90 nM, 2.00 nM, 2.50 nM, 3.00 nM,3.50 nM, 0.004 μM, 0.006 μM, 0.008 μM, 0.010 μM, 0.012 μM, 0.014 μM,0.015 μM, 0.016 μM, 0.017 μM, 0.018 μM, 0.019 μM, 0.020 μM, 0.021 μM,0.022 μM, 0.023 μM, 0.024 μM, or 0.025 μM, or within a range defined byany two of the preceding values, for the period of time. In someembodiments, the amount of IL-10 is about 0.100 nM, 0.110 nM, 0.120 nM,0.130 nM, 0.140 nM, 0.150 nM, 0.160 nM, 0.170 nM, 0.180 nM, 0.190 nM,0.200 nM, 0.220 nM, 0.240 nM, 0.260 nM, 0.280 nM, 0.300 nM, 0.350 nM,0.400 nM, 0.450 nM, 0.500 nM, 0.550 nM, 0.600 nM, 0.650 nM, 0.700 nM,0.750 nM, 0.800 nM, 0.850 nM, 0.900 nM, 0.950 nM, 1.00 nM, 1.10 nM, 1.20nM, 1.30 nM, 1.40 nM, 1.50 nM, 1.60 nM, 1.70 nM, 1.80 nM, 1.90 nM, 2.00nM, 2.50 nM, 3.00 nM, 3.50 nM, 0.004 μM, 0.006 μM, 0.008 μM, 0.010 μM,0.012 μM, 0.014 μM, 0.015 μM, 0.016 μM, 0.017 μM, 0.018 μM, 0.019 μM,0.020 μM, 0.021 μM, 0.022 μM, 0.023 μM, 0.024 μM, or 0.025 μM, or withina range defined by any two of the preceding values, for the period oftime. In some embodiments, the amount of IL-10 is about 0.200 nM, 0.220nM, 0.240 nM, 0.260 nM, 0.280 nM, 0.300 nM, 0.350 nM, 0.400 nM, 0.450nM, 0.500 nM, 0.550 nM, 0.600 nM, 0.650 nM, 0.700 nM, 0.750 nM, 0.800nM, 0.850 nM, 0.900 nM, 0.950 nM, 1.00 nM, 1.10 nM, 1.20 nM, 1.30 nM,1.40 nM, 1.50 nM, 1.60 nM, 1.70 nM, 1.80 nM, 1.90 nM, 2.00 nM, 2.50 nM,3.00 nM, 3.50 nM, 0.004 μM, 0.006 μM, 0.008 μM, 0.010 μM, 0.012 μM,0.014 μM, 0.015 μM, 0.016 μM, 0.017 μM, 0.018 μM, 0.019 μM, 0.020 μM,0.021 μM, 0.022 μM, 0.023 μM, 0.024 μM, or 0.025 μM, or within a rangedefined by any two of the preceding values, for the period of time. Insome embodiments, the amount of IL-10 is about 0.300 nM, 0.350 nM, 0.400nM, 0.450 nM, 0.500 nM, 0.550 nM, 0.600 nM, 0.650 nM, 0.700 nM, 0.750nM, 0.800 nM, 0.850 nM, 0.900 nM, 0.950 nM, 1.00 nM, 1.10 nM, 1.20 nM,1.30 nM, 1.40 nM, 1.50 nM, 1.60 nM, 1.70 nM, 1.80 nM, 1.90 nM, 2.00 nM,2.50 nM, 3.00 nM, 3.50 nM, 0.004 μM, 0.006 μM, 0.008 μM, 0.010 μM, 0.012μM, 0.014 μM, 0.015 μM, 0.016 μM, 0.017 μM, 0.018 μM, 0.019 μM, 0.020μM, 0.021 μM, 0.022 μM, 0.023 μM, 0.024 μM, or 0.025 μM, or within arange defined by any two of the preceding values, for the period oftime. In some embodiments, the amount of IL-10 is about 0.400 nM, 0.450nM, 0.500 nM, 0.550 nM, 0.600 nM, 0.650 nM, 0.700 nM, 0.750 nM, 0.800nM, 0.850 nM, 0.900 nM, 0.950 nM, 1.00 nM, 1.10 nM, 1.20 nM, 1.30 nM,1.40 nM, 1.50 nM, 1.60 nM, 1.70 nM, 1.80 nM, 1.90 nM, 2.00 nM, 2.50 nM,3.00 nM, 3.50 nM, 0.004 μM, 0.006 μM, 0.008 μM, 0.010 μM, 0.012 μM,0.014 μM, 0.015 μM, 0.016 μM, 0.017 μM, 0.018 μM, 0.019 μM, 0.020 μM,0.021 μM, 0.022 μM, 0.023 μM, 0.024 μM, or 0.025 μM, or within a rangedefined by any two of the preceding values, for the period of time. Insome embodiments, the amount of IL-10 is about 0.500 nM, 0.550 nM, 0.600nM, 0.650 nM, 0.700 nM, 0.750 nM, 0.800 nM, 0.850 nM, 0.900 nM, 0.950nM, 1.00 nM, 1.10 nM, 1.20 nM, 1.30 nM, 1.40 nM, 1.50 nM, 1.60 nM, 1.70nM, 1.80 nM, 1.90 nM, 2.00 nM, 2.50 nM, 3.00 nM, 3.50 nM, 0.004 μM,0.006 μM, 0.008 μM, 0.010 μM, 0.012 μM, 0.014 μM, or 0.015 μM for theperiod of time or within a range defined by any two of the precedingvalues for the period of time. In some embodiments, the amount of IL-10is about 0.600 nM, 0.650 nM, 0.700 nM, 0.750 nM, 0.800 nM, 0.850 nM,0.900 nM, 0.950 nM, 1.00 nM, 1.10 nM, 1.20 nM, 1.30 nM, 1.40 nM, 1.50nM, 1.60 nM, 1.70 nM, 1.80 nM, 1.90 nM, 2.00 nM, 2.50 nM, 3.00 nM, 3.50nM, 0.004 μM, 0.006 μM, 0.008 μM, 0.010 μM, 0.012 μM, 0.014 μM, or 0.015μM for the period of time or within a range defined by any two of thepreceding values for the period of time. In some embodiments, the amountof IL-10 is about 0.700 nM, 0.750 nM, 0.800 nM, 0.850 nM, 0.900 nM,0.950 nM, 1.00 nM, 1.10 nM, 1.20 nM, 1.30 nM, 1.40 nM, 1.50 nM, 1.60 nM,1.70 nM, 1.80 nM, 1.90 nM, 2.00 nM, 2.50 nM, 3.00 nM, 3.50 nM, 0.004 μM,0.006 μM, 0.008 μM, 0.010 μM, 0.012 μM, 0.014 μM, or 0.015 μM for theperiod of time or within a range defined by any two of the precedingvalues for the period of time. In some embodiments, the amount of IL-10is about 0.800 nM, 0.850 nM, 0.900 nM, 0.950 nM, 1.00 nM, 1.10 nM, 1.20nM, 1.30 nM, 1.40 nM, 1.50 nM, 1.60 nM, 1.70 nM, 1.80 nM, 1.90 nM, 2.00nM, 2.50 nM, 3.00 nM, 3.50 nM, 0.004 μM, 0.006 μM, 0.008 μM, 0.010 μM,0.012 μM, 0.014 μM, or 0.015 μM for the period of time or within a rangedefined by any two of the preceding values for the period of time. Insome embodiments, the amount of IL-10 is about 0.900 nM, 0.950 nM, 1.00nM, 1.10 nM, 1.20 nM, 1.30 nM, 1.40 nM, 1.50 nM, 1.60 nM, 1.70 nM, 1.80nM, 1.90 nM, 2.00 nM, 2.50 nM, 3.00 nM, 3.50 nM, 0.004 μM, 0.006 μM,0.008 μM, 0.010 μM, 0.012 μM, 0.014 μM, or 0.015 μM for the period oftime or within a range defined by any two of the preceding values forthe period of time. In some embodiments, the amount of IL-10 is about1.00 nM, 1.10 nM, 1.20 nM, 1.30 nM, 1.40 nM, 1.50 nM, 1.60 nM, 1.70 nM,1.80 nM, 1.90 nM, 2.00 nM, 2.50 nM, 3.00 nM, 3.50 nM, 0.004 μM, 0.006μM, 0.008 μM, 0.010 μM, 0.012 μM, 0.014 μM, or 0.015 μM for the periodof time or within a range defined by any two of the preceding values forthe period of time. In some embodiments, the amount of IL-10 is about2.00 nM, 2.50 nM, 3.00 nM, 3.50 nM, 0.004 μM, 0.006 μM, 0.008 μM, 0.010μM, 0.012 μM, 0.014 μM, or 0.015 μM for the period of time or within arange defined by any two of the preceding values for the period of time.In some embodiments, the amount of IL-10 is about 3.00 nM, 3.50 nM,0.004 μM, 0.006 μM, 0.008 μM, 0.010 μM, 0.012 μM, 0.014 μM, or 0.015 μMfor the period of time or within a range defined by any two of thepreceding values for the period of time. In some embodiments, the amountof IL-10 is about 0.004 μM, 0.006 μM, 0.008 μM, 0.010 μM, 0.012 μM,0.014 μM, or 0.015 μM for the period of time or within a range definedby any two of the preceding values for the period of time. In someembodiments, the amount of IL-10 in the dermis, epidermis, woundmicroenvironment, wound tissue homogenate, serum, plasma, or otherrelevant anatomical site for increased fibrosis is from about 0.015 nM,0.020 nM, 0.025 nM, 0.030 nM, 0.035 nM, 0.040 nM, 0.045 nM, 0.050 nM,0.055 nM, 0.060 nM, 0.065 nM, 0.070 nM, 0.075 nM, 0.080 nM, 0.085 nM,0.090 nM, 0.095 nM, 0.100 nM, 0.110 nM, 0.120 nM, 0.130 nM, 0.140 nM,0.150 nM, 0.160 nM, 0.170 nM, 0.180 nM, 0.190 nM, 0.200 nM, 0.220 nM,0.240 nM, 0.260 nM, 0.280 nM, 0.300 nM, 0.350 nM, 0.400 nM, 0.450 nM,0.500 nM, 0.550 nM, 0.600 nM, 0.650 nM, 0.700 nM, 0.750 nM, 0.800 nM,0.850 nM, 0.900 nM, 0.950 nM, 1.00 nM, 1.10 nM, 1.20 nM, 1.30 nM, 1.40nM, 1.50 nM, 1.60 nM, 1.70 nM, 1.80 nM, 1.90 nM, or 2.00 nM, or within arange defined by any two of the preceding values, for the period oftime. In some embodiments, the amount of IL-10 in the dermis, epidermis,wound microenvironment, wound tissue homogenate, serum, plasma, or otherrelevant anatomical site for increased fibrosis is from about 0.015 nM,0.020 nM, 0.025 nM, 0.030 nM, 0.035 nM, 0.040 nM, 0.045 nM, 0.050 nM,0.055 nM, 0.060 nM, 0.065 nM, 0.070 nM, 0.075 nM, 0.080 nM, 0.085 nM,0.090 nM, 0.095 nM, 0.100 nM, 0.110 nM, 0.120 nM, 0.130 nM, 0.140 nM,0.150 nM, 0.160 nM, 0.170 nM, 0.180 nM, 0.190 nM, 0.200 nM, 0.220 nM,0.240 nM, 0.260 nM, 0.280 nM, 0.300 nM, 0.350 nM, 0.400 nM, 0.450 nM,0.500 nM, 0.550 nM, 0.600 nM, 0.650 nM, 0.700 nM, 0.750 nM, 0.800 nM,0.850 nM, 0.900 nM, 0.950 nM, or 1.00 nM, or within a range defined byany two of the preceding values, for the period of time. In someembodiments, the amount of IL-10 in the dermis, epidermis, woundmicroenvironment, wound tissue homogenate, serum, plasma, or otherrelevant anatomical site for increased fibrosis is from about 0.015 nM,0.020 nM, 0.025 nM, 0.030 nM, 0.035 nM, 0.040 nM, 0.045 nM, 0.050 nM,0.055 nM, 0.060 nM, 0.065 nM, 0.070 nM, 0.075 nM, 0.080 nM, 0.085 nM,0.090 nM, 0.095 nM, 0.100 nM, 0.110 nM, 0.120 nM, 0.130 nM, 0.140 nM,0.150 nM, 0.160 nM, 0.170 nM, 0.180 nM, 0.190 nM, 0.200 nM, 0.220 nM,0.240 nM, 0.260 nM, 0.280 nM, 0.300 nM, 0.350 nM, 0.400 nM, 0.450 nM, or0.500 nM, or within a range defined by any two of the preceding values,for the period of time. In some embodiments, the amount of IL-10 in thedermis, epidermis, wound microenvironment, wound tissue homogenate,serum, plasma, or other relevant anatomical site for increased fibrosisis from about 0.015 nM, 0.020 nM, 0.025 nM, 0.030 nM, 0.035 nM, 0.040nM, 0.045 nM, 0.050 nM, 0.055 nM, 0.060 nM, 0.065 nM, 0.070 nM, 0.075nM, 0.080 nM, 0.085 nM, 0.090 nM, 0.095 nM, 0.100 nM, 0.110 nM, 0.120nM, 0.130 nM, 0.140 nM, 0.150 nM, 0.160 nM, 0.170 nM, 0.180 nM, 0.190nM, or 0.200 nM, or within a range defined by any two of the precedingvalues, for the period of time. In some embodiments, the period of timemay be measured starting from initial administration of the composition.In some embodiments, the period of time is up to about 0.5, 1, 2, 3, 4,5, 6, 7, 8, 9, 10, 12, 15, 20, 25 or 30 days or up to a number thatfalls within a range defined by any two of the preceding values. In someembodiments, the period of time may be the first seven days afteradministration of IL-10. In some embodiments, the period of time may bethe first 5 days after administration of IL-10. In some embodiments, theperiod of time may be the first three days after administration ofIL-10.

In some embodiments, the amount of IL-10 in the dermis, epidermis, woundmicroenvironment, wound tissue homogenate, serum, plasma, or otherrelevant anatomical site for increased fibrosis is from about 0.015 nMto 0.015 μM for a sustained release time period. In some embodiments,the amount of IL-10 is about 0.015 nM, 0.04 nM, 0.08 nM, 0.12 nM, 0.16nM, or 0.2 nM, or within a range defined by any two of the precedingvalues, for the sustained release time period. In some embodiments, thesustained release time period may be measure starting from initialadministration of the composition. In some embodiments, the sustainedrelease time period is up to about 1, 2, 3, 5, 7, 10, 12, 15, 18, 20 or30 days or a range defined by any two of the preceding values. In someembodiments, the sustained release time period may be up to seven daysafter administration. In some embodiments, the sustained release timeperiod may be from 1 day to up to 14 days after administration of IL-10.In some embodiments, the sustained release time period may be from 2days to up to 14 days after administration of IL-10. In someembodiments, the sustained release time period may be from 2 days to upto seven days after administration of IL-10. In some embodiments, thesustained release time period may be from after the first day to up toseven days after administration of IL-10.

In some embodiments, the amount of IL-10 in the dermis, epidermis, woundmicroenvironment, wound tissue homogenate, serum, plasma, or otherrelevant anatomical site for increased fibrosis is from about 0.002 μMto 0.015 μM for a bolus time period and between 0.015 nM to about 0.2 nMfor a sustained release time period. In some embodiments, the amount ofIL-10 is about 0.002 μM, 0.004 μM, 0.006 μM, 0.008 μM, 0.010 μM, 0.012μM, 0.014 μM, or 0.015 μM for the bolus time period or within a rangedefined by any two of the preceding values for the bolus time period. Insome embodiments, the amount of IL-10 is about 0.015 nM, 0.04 nM, 0.08nM, 0.12 nM, 0.16 nM, or 0.2 nM for the sustained release time period orwithin a range defined by any two of the preceding values for thesustained release time period. In some embodiments, the bolus timeperiod may be measured starting from initial administration of thecomposition. In some embodiments, the sustained release time period maybe measure starting from initial administration of the composition. Insome embodiments, the bolus time period is up to about 0.5, 1, 2, 3, 5,or 7 days or up to a number that falls within a range defined by any twoof the preceding values. In some embodiments, the sustained release timeperiod is up to about 1, 2, 3, 5, 7, 10, 12, 15, 18, 20 or 30 days or arange defined by any two of the preceding values. In some embodiments,the maximum concentration of IL-10 during the bolus time period may begreater than the maximum concentration of IL-10 during the sustainedrelease time. In some embodiments, the bolus time period may be thefirst three days after administration of IL-10. In some embodiments, thebolus time period may be the first two days after administration ofIL-10. In some embodiments, the sustained release time period may be upto seven days after administration. In some embodiments, the sustainedrelease time period may be from 1 day to up to 14 days afteradministration of IL-10. In some embodiments, the sustained release timeperiod may be from 2 days to up to 14 days after administration ofIL-10. In some embodiments, the sustained release time period may befrom 2 days to up to seven days after administration of IL-10. In someembodiments, the bolus time period may be the first day afteradministration of IL-10 and the sustained release time period may befrom after the first day to up to seven days after administration ofIL-10.

The biocompatible compositions provided herein comprise IL-10. In someembodiments, the amount of IL-10 in the composition is from about 0.017μM to about 0.035 μM. In some embodiments, the amount of IL-10 in thecomposition is about 0.017 μM, 0.019 μM, 0.021 μM, 0.023 μM, 0.025 μM,0.027 μM, 0.029 μM, 0.031 μM, 0.033 μM, or 0.055 μM, or within a rangedefined by any two of the preceding values.

In some embodiments, the incision or wound site is at a dermal layer orepidermis or other relevant anatomical site for increased fibrosis.

In some embodiments, the incision or wound site includes a dermal layeror epidermis or other relevant anatomical site for increased fibrosis.

In some embodiments, the wound is restored to a condition substantiallyidentical to the surrounding tissue within a second period of time frominitial administration of the composition. In some embodiments, thesecond period of time is at least about 1 day. In some embodiments, thesecond period of time is at least about 2 days. In some embodiments, thesecond period of time is at least about 3 days. In some embodiments, thesecond period of time is at least about 4 days. In some embodiments, thesecond period of time is about 2 to about 30 days. In some embodiments,the second period of time is about 3 to about 7 days. In someembodiments, the second period of time is at least about 1, 2, 3, 5, 7,10, 12, 15, 18, 20 or 30 days or a range defined by any two of thepreceding values.

In some embodiments, the wound is a trauma wound, and the composition isadministered at the wound site within a third period of time frominitial wound formation. In some embodiments, the third period of timeis within about 1 minute. In some embodiments, the third period of timeis within about 5 minutes. In some embodiments, the third period of timeis within about 30 minutes. In some embodiments, the third period oftime is within about 1 hour. In some embodiments, the third period of iswithin about 2 hours. In some embodiments, the third period of is withinabout 4 hours. In some embodiments, the third period of is within about6 hours. In some embodiments, the third period of is within about 12hours. In some embodiments, the third period of is within about 24hours. In some embodiments, the third period of time is within about 1minute, 5 minutes, 30 minutes, 60 minutes, 2 hours, 4 hours, 6 hours, or24 hours or within a range defined by any two of the preceding values.

In some embodiments, the wound may be a hypertrophic scar, keloid, burncontracture, and the composition is administered at the wound sitewithin a third period of time from initial wound formation. In someembodiments, the third period of time is within about 5 minutes. In someembodiments, the third period of time is within about 30 minutes. Insome embodiments, the third period of time is within about 1 hour. Insome embodiments, the third period of time is within about 2 hours. Insome embodiments, the third period of time is within about 4 hours. Insome embodiments, the third period of time is within about 6 hours. Insome embodiments, the third period of time is within about 12 hours. Insome embodiments, the third period of time is within about 24 hours. Insome embodiments, the third period of time is within about 1 minute, 5minutes, 30 minutes, 60 minutes, 2 hours, 4 hours, 6 hours, or 24 hoursor within a range defined by any two of the preceding values.

In some embodiments, the area of application is an anatomic specificarea, such as the intraabdominal cavity for adhesions, the kidney, lungor liver for organ specific fibrosis, and the composition isadministered at the site of fibroplasia within a third period of timefrom initial scar formation. In some embodiments, the third period oftime is within about 5 minutes. In some embodiments, the third period oftime is within about 30 minutes. In some embodiments, the third periodof time is within about 1 hour. In some embodiments, the third period oftime is within about 2 hours. In some embodiments, the third period oftime is within about 4 hours. In some embodiments, the third period oftime is within about 6 hours. In some embodiments, the third period ofis within about 12 hours. In some embodiments, the third period of timeis within about 24 hours. In some embodiments, the third period of timeis within about 1 minute, 5 minutes, 30 minutes, 60 minutes, 2 hours, 4hours, 6 hours, or 24 hours or within a range defined by any two of thepreceding values. Some such embodiments provide a method for preventingor reducing scarring or process characterized by excessive fibroplasiaincluding but not limited to pathologic scars and keloids.

In some embodiments, the method further comprises making a surgicalincision, wherein the composition is administered at the incision.

Some embodiments provide a method of evaluating a composition fortreating a wound including: providing a dosage of the composition to awound in a statistically relevant number of animals; and evaluating thewound in each animal after a period of time using an Assessment Scalevalue to obtain an Assessment Scale score, wherein said Assessment Scalescore is based on the measurement of at least 2 parameters selected fromthe group consisting of i) the quantification of topography, ii)epidermal height, and iii) the nuclear orientation of the basalkeratinocytes in the epidermis; and iv) the quantification of the scararea, v) dermal appendages, and vi) vascularity (vessel density) in thedermis of the scars. In some embodiments, each parameter is calculatedto provide an Assessment Scale value (INDEX), wherein an AssessmentScale score is calculated by (^(n)Σ INDEX/n)×100 where n is the numberof parameters being evaluated. In some embodiments, the animals aremice. In some embodiments, the statistically relevant number is three ormore. In some embodiments, the period of time is 20 days. In someembodiments, the dosage is a single dosage. In some embodiments, thecomposition comprises IL-10. In some embodiments, the compositioncomprises IL-10 and a biodegradable support scaffold. In someembodiments, n is 2, 3, 4, 5 or 6. In some embodiments, n is 3. In someembodiments, n is 4. In some embodiments, n is 5. In some embodiments, nis 6.

Compositions

Some embodiments provide an extended release biocompatible compositionfor preventing or reducing scarring of an incision or wound site in asubject, comprising: a biodegradable support scaffold; and IL-10,wherein the amount of IL-10 in the composition is from about 0.05 ng/μLto about 1500 ng/μL. In some embodiments, the composition may be ahydrogel.

In some embodiments, the amount of IL-10 in the composition is fromabout 1 ng/μL to about 1000 ng/μL. In some embodiments, the amount ofIL-10 in the composition is from about 2 ng/μL to about 500 ng/μL. Insome embodiments, the amount of IL-10 in the composition is from about 4ng/μL to about 250 ng/mL. In some embodiments, the amount of IL-10 inthe composition is from about 6 ng/μL to about 125 ng/μL. In someembodiments, the amount of IL-10 in the composition is from about 8ng/μL to about 100 ng/μL. In some embodiments, the amount of IL-10 inthe composition is from about 10 ng/μL to about 75 ng/μL. In someembodiments, the amount of IL-10 in the composition is from about 20ng/μL to about 45 ng/μL.

In some embodiments, the amount of IL-10 in the composition is fromabout 5 ng to about 5000 ng. In some embodiments, the amount of IL-10 inthe composition is from about 50 ng to about 2500 ng. In someembodiments, the amount of IL-10 in the composition is from about 100 ngto about 1250 ng.

In some embodiments, the composition is from about 0.1 mg to about 1 g.In some embodiments, the composition is from about 0.1 mg to about 500mg. In some embodiments, the composition is from about 0.1 mg to about250 mg. In some embodiments, the composition is from about 0.1 mg toabout 125 mg. In some embodiments, the composition is from about 0.1 mgto about 80 mg. In some embodiments, the composition is from about 0.1mg to about 40 mg. In some embodiments, the composition is from about0.1 mg to about 20 mg.

The daily dosage of IL-10 may be varied over a wide range; e.g., fromabout 0.1 μg to about 10,000 μg per adult human per day.

Therapeutically effective dosages of IL-10 can range from 0.1 μg toabout 0.5 μg per dose, from about 0.5 μg to about 1.0 μg per dose, fromabout 1.0 μg per dose to about 5.0 μg per dose, from about 5.0 μg toabout 10 μg per dose, from about 10 μg to about 20 μg per dose, fromabout 20 μg per dose to about 30 μg per dose, from about 30 μg per doseto about 40 μg per dose, from about 40 μg per dose to about 50 μg perdose, from about 50 μg per dose to about 60 μg per dose, from about 60μg per dose to about 70 μg per dose, from about 70 μg to about 80 μg perdose, from about 80 μg per dose to about 100 μg per dose, from about 100μg to about 150 μg per dose, from about 150 μg to about 200 μg per dose,from about 200 μg per dose to about 250 μg per dose, from about 250 μgto about 300 μg per dose, from about 300 μg to about 400 μg per dose,from about 400 μg to about 500 μg per dose, from about 500 μg to about600 μg per dose, from about 600 μg to about 700 μg per dose, from about700 μg to about 800 μg per dose, from about 800 μg to about 900 μg perdose, from about 900 μg to about 1000 μg per dose, from about 1 mg toabout 10 mg per dose. An effective amount of IL-10 is ordinarilysupplied at a dosage level of from about 0.01 mg/cm² to about 150 mg/cm²per day. Typically, the range is from about 0.1 to about 80 mg/cm² perday, and especially from about 0.2 mg/cm² to about 40 mg/cm² per day. Insome embodiments, the composition may be administered on a regimen ofabout 1 to about 10 times per day, or continuous infusion for a periodof from about 1, 5, 10, 15, 30 or 60 minutes, or 1, 2, 3, 5, 7, 10, 12,15, 18, 20 or 24 hours or a range defined by any two of the precedingvalues. In a typical embodiment, the composition may be administeredonce.

Some embodiments provide an extended release biocompatible compositioncomprising from about 1 mg/mL to about 300 mg/mL IL-10 having from about15% release to about 50% release of IL-10 relative to the initial amountof IL-10 in the initial composition within 24 hours of initialadministration. In some embodiments the extended release biocompatiblecomposition comprising from about 1 mg/mL to about 300 mg/mL IL-10 mayhave about 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45% or 50%, or withina range defined by any two of the preceding values, release of IL-10relative to the initial amount of IL-10 in the initial compositionwithin 24 hours of initial administration. In some embodiments theextended release biocompatible composition comprising from about 1 mg/mLto about 300 mg/mL IL-10 may have 0.1%, 0.2%, 0.4%, 0.8%, 1.2%, 1.6%,2%, 2.4%, 2.8%, 3.2%, 3.6%, 4.0%, 4.4%, 4.8%, 5.2%, 5.6%, 6.0%, 6.4%,6.8%, 7.2%, 7.6%, 8.0%, 8.4%, 8.8%, 9.2%, 9.6%, or 10%, or within arange defined by any two of the preceding values, release of IL-10relative to the initial amount of IL-10 in the initial composition fromthe time period of about 24 hours to about 48 hours of initialadministration. In some embodiments the extended release biocompatiblecomposition comprising from about 1 mg/mL to about 300 mg/mL IL-10 mayhave 0.01%, 0.02%, 0.04%, 0.08%, 0.12%, 0.16%, 0.2%, 0.24%, 0.28%,0.32%, 0.36%, 0.40%, 0.44%, 0.48%, 0.52%, 0.56%, 0.6%, 0.64%, 0.68%,0.72%, 0.76%, 0.80%, 0.84%, 0.88%, 0.92%, 0.96%, or 1.0%, or within arange defined by any two of the preceding values, release of IL-10relative to the initial amount of IL-10 in the initial composition fromthe time period of about 48 hours to about 72 hours of initialadministration. In some embodiments the extended release biocompatiblecomposition comprising from about 1 mg/mL to about 300 mg/mL IL-10 mayhave 0.001%, 0.002%, 0.004%, 0.008%, 0.012%, 0.016%, 0.02%, 0.024%,0.028%, 0.032%, 0.036%, 0.040%, 0.044%, 0.048%, 0.052%, 0.056%, 0.06%,0.064%, 0.068%, 0.072%, 0.076%, 0.080%, 0.084%, 0.088%, 0.092%, 0.096%,0.1%, 0.12%, 0.16%, 0.2%, 0.24%, 0.28%, 0.32%, 0.36%, 0.40%, 0.44%,0.48%, 0.52%, 0.56%, 0.6%, 0.64%, 0.68%, 0.72%, 0.76%, 0.80%, 0.84%,0.88%, 0.92%, 0.96%, or 1.0%, or within a range defined by any two ofthe preceding values, release of IL-10 relative to the initial amount ofIL-10 in the initial composition from the time period of about 72 hoursto about 96 hours of initial administration. In some embodiments theextended release biocompatible composition comprising from about 1 mg/mLto about 300 mg/mL IL-10 may have 0.001%, 0.002%, 0.004%, 0.008%,0.012%, 0.016%, 0.02%, 0.024%, 0.028%, 0.032%, 0.036%, 0.040%, 0.044%,0.048%, 0.052%, 0.056%, 0.06%, 0.064%, 0.068%, 0.072%, 0.076%, 0.080%,0.084%, 0.088%, 0.092%, 0.096%, 0.1%, 0.12%, 0.16%, 0.2%, 0.24%, 0.28%,0.32%, 0.36%, 0.40%, 0.44%, 0.48%, 0.52%, 0.56%, 0.6%, 0.64%, 0.68%,0.72%, 0.76%, 0.80%, 0.84%, 0.88%, 0.92%, 0.96%, or 1.0%, or within arange defined by any two of the preceding values, release of IL-10relative to the initial amount of IL-10 in the initial composition fromthe time period of about 96 hours to about 120 hours of initialadministration. In some embodiments the extended release biocompatiblecomposition comprising from about 1 mg/mL to about 300 mg/mL IL-10 mayhave 0.001%, 0.002%, 0.004%, 0.008%, 0.012%, 0.016%, 0.02%, 0.024%,0.028%, 0.032%, 0.036%, 0.040%, 0.044%, 0.048%, 0.052%, 0.056%, 0.06%,0.064%, 0.068%, 0.072%, 0.076%, 0.080%, 0.084%, 0.088%, 0.092%, 0.096%,0.1%, 0.12%, 0.16%, 0.2%, 0.24%, 0.28%, 0.32%, 0.36%, 0.40%, 0.44%,0.48%, 0.52%, 0.56%, 0.6%, 0.64%, 0.68%, 0.72%, 0.76%, 0.80%, 0.84%,0.88%, 0.92%, 0.96%, or 1.0%, or within a range defined by any two ofthe preceding values, release of IL-10 relative to the initial amount ofIL-10 in the initial composition from the time period of about 120 hoursto about 144 hours of initial administration. In some embodiments theextended release biocompatible composition comprising from about 1 mg/mLto about 300 mg/mL IL-10 may have 0.001%, 0.002%, 0.004%, 0.008%,0.012%, 0.016%, 0.02%, 0.024%, 0.028%, 0.032%, 0.036%, 0.040%, 0.044%,0.048%, 0.052%, 0.056%, 0.06%, 0.064%, 0.068%, 0.072%, 0.076%, 0.080%,0.084%, 0.088%, 0.092%, 0.096%, 0.1%, 0.12%, 0.16%, 0.2%, 0.24%, 0.28%,0.32%, 0.36%, 0.40%, 0.44%, 0.48%, 0.52%, 0.56%, 0.6%, 0.64%, 0.68%,0.72%, 0.76%, 0.80%, 0.84%, 0.88%, 0.92%, 0.96%, or 1.0%, or within arange defined by any two of the preceding values, release of IL-10relative to the initial amount of IL-10 in the initial composition fromthe time period of about 144 hours to about 168 hours of initialadministration. In some embodiments the amount of IL-10 released withina time period may be established using the following protocol:

PROTOCOL A

Extracel-HP™ HMW-HA hydrogel (Glycosan a division of BioTime, Inc.,Alameda, Calif.) including heparin and IL-10 (800 ng in 25 μL for ineach well of a 48-well dish) is placed in media (250 μL) such asDulbecco's Modified Eagle Medium (Life Technologies Corporation,Carlsbad, Calif.). After around 24 hours the media from each well isremoved and separately maintained for analysis. Fresh media (250 μL) isadded to each well. The amount of IL-10 in each well is measured byELISA. This process is repeated every 24 hours for a total of sevendays. In some embodiments, the composition can have, for example, 25percent release of IL-10 within 24 hours evaluated using PROTOCOL A, 50percent release of IL-10 within 48 hours evaluated using PROTOCOL A, 75percent release of IL-10 within 72 hours evaluated using PROTOCOL A.

In some embodiments, the composition may include a biodegradable supportscaffold including at least one of hyaluronan, a hyaluronan moiety,heparin, heparan sulfate, collagen, PEG, a PEG moiety or a cross-linker,as described herein. In some embodiments, the composition may include abiodegradable support scaffold including at least two of hyaluronan, ahyaluronan moiety, heparin, heparan sulfate, collagen, PEG, a PEG moietyor a cross-linker. In some embodiments, the composition may include abiodegradable support scaffold including at least three of hyaluronan, ahyaluronan moiety, heparin, heparan sulfate, collagen, PEG, a PEG moietyor a cross-linker. In some embodiments, the composition may include abiodegradable support scaffold including at least four of hyaluronan, ahyaluronan moiety, heparin, heparan sulfate, collagen, PEG, a PEG moietyor a cross-linker. In some embodiments, the composition may be ahydrogel.

The composition can be formulated readily, for example, by combining thebiodegradable support scaffold with any suitable pharmaceuticallyacceptable excipient for example, but not limited to, binders, diluents,disintegrants, lubricants, fillers, carriers, and the like, as set forthbelow. Such compositions can be prepared for storage and for subsequentprocessing.

Acceptable excipients for therapeutic use are well known in thepharmaceutical art, and are described, for example, in Handbook ofPharmaceutical Excipients, 5th edition (Raymond C Rowe, Paul J Sheskeyand Siân C Owen, eds. 2005), and Remington: The Science and Practice ofPharmacy, 21st edition (Lippincott Williams & Wilkins, 2005), each ofwhich is hereby incorporated in its entirety. The term “carrier”material or “excipient” herein can mean any substance, not itself atherapeutic agent, used as a carrier and/or diluent and/or adjuvant, orvehicle for delivery of a therapeutic agent to a subject or added to apharmaceutical composition to improve its handling or storage propertiesor to permit or facilitate formation of a dose unit of the compositioninto a gel, lotion, cream, ointment, solid, semi-solid, or a discretearticle such as a capsule, tablet, film coated tablet, caplet, gel cap,pill, pellet, bead, and the like. In some embodiments, the compositionmay be a hydrogel. Excipients can include, by way of illustration andnot limitation, diluents, disintegrants, binding agents, wetting agents,polymers, lubricants, glidants, substances added to mask or counteract adisagreeable taste or odor, flavors, colorants, fragrances, andsubstances added to improve appearance of the composition.

Acceptable excipients include, for example, but are not limited to,lactose, sucrose, starch powder, maize starch or derivatives thereof,cellulose esters of alkanoic acids, cellulose alkyl esters, talc,stearic acid, magnesium stearate, magnesium oxide, sodium and calciumsalts of phosphoric and sulfuric acids, gelatin, acacia gum, sodiumalginate, polyvinyl-pyrrolidone, and/or polyvinyl alcohol, saline,dextrose, mannitol, lactose, lecithin, albumin, sodium glutamate,cysteine hydrochloride, and the like. Suitable excipients for thepreparation of solutions and syrups include, without limitation, water,polyols, sucrose, invert sugar and glucose.

Any of the foregoing mixtures can be appropriate in treatments andtherapies in accordance with the embodiments disclosed herein, providedthat the active ingredient in the formulation is not inactivated by theformulation and the formulation is physiologically compatible andtolerable with the route of administration. See also Baldrick P.“Pharmaceutical excipient development: the need for preclinicalguidance.” Regul. Toxicol. Pharmacol. 32(2):210-8 (2000), Charman W N“Lipids, lipophilic drugs, and oral drug delivery-some emergingconcepts.” J Pharm Sci 0.89(8):967-78 (2000), and the citations thereinfor additional information related to formulations, excipients andcarriers well known to pharmaceutical chemists.

In some embodiments, one or more, or any combination of the listedexcipients can be specifically included or excluded from theformulations and/or methods disclosed herein.

In some embodiments, the formulation can be in form suitable for bolusadministration.

As will be appreciated by those of skill in the art, the amounts ofexcipients will be determined by drug dosage and dosage form size. Insome embodiments, the dosage form size of the composition is in therange of about 5 μL to about 1 liter. This dosage form weight isarbitrary and one skilled in the art will realize that a range ofweights can be made and are encompassed. The preferred dosage form sizeof the composition is 500 μL to 10 mL, more preferably 750 μL to 5 mL,more preferably 1 mL to 5 mL, with the preferred dosage form being aviscous solution.

Methods of Administration

In any of the embodiments, administration can be by bolusadministration, e.g., subcutaneous bolus administration, intramuscularbolus administration, intradermal bolus administration and the like. Inany of the embodiments, administration can be by infusion, e.g.,subcutaneous infusion, intramuscular infusion, intradermal infusion, andthe like. In some embodiments, administration can be by direct tissueinjections. In some embodiments, the composition may include a hydrogel.

Administration, preferably intradermal administration, of apharmaceutical composition including a sustained release formulation asdisclosed and described herein is accomplished using standard methodsand devices, e.g., pens, injector systems, needle and syringe, anintradermal injection system, and the like. In some embodiments,intradermal administration can be achieved by bolus delivery by needleand syringe. In some embodiments, the composition may be a viscous gel,liquid, settable liquid, or semi-solid. In some embodiments, thecomposition may include a hydrogel. In some embodiments, the settableliquid may set to afford a solid or semi-solid upon administration tothe wound.

Solutions or suspensions used for parenteral, intradermal, subcutaneous,intramuscular or topical application can include any of the followingcomponents: a sterile diluent, such as water for injection, salinesolution, fixed oil, polyethylene glycol, glycerine, propylene glycol orother synthetic solvent; antimicrobial agents, such as benzyl alcoholand methyl parabens; antioxidants, such as ascorbic acid and sodiumbisulfite; cheating agents, such as ethylenediaminetetraacetic acid(EDTA); buffers, such as acetates, citrates and phosphates; and agentsfor the adjustment of tonicity, including, but not limited to sodiumchloride, calcium chloride, magnesium chloride, dextrose, glycerol orboric acid. Parenteral preparations can be enclosed in ampoules,disposable syringes or single or multiple dose vials made of glass,plastic or other suitable material.

Parenteral administration of a pharmaceutical compositions including asustained release formulation as disclosed and described herein,generally characterized by injection, either subcutaneously,intradermally, or intramuscularly is also contemplated herein. In someembodiments, parenteral administration of a pharmaceutical compositionsincluding a sustained release formulation as disclosed and describedherein includes direct tissue injections. Injectables can be prepared inconventional forms, either as liquid solutions or suspensions; solidforms suitable for solution or suspension in liquid prior to injection,or as emulsions. Suitable excipients are, for example, water, saline,dextrose, glycerol or ethanol. In addition, if desired, thepharmaceutical compositions to be administered can also contain minoramounts of non-toxic auxiliary substances such as wetting or emulsifyingagents, pH buffering agents, stabilizers, solubility enhancers, andother such agents, such as, for example, sodium acetate, sorbitanmonolaurate, triethanolamine oleate and cyclodextrins.

Parenteral administration of the compositions includes subcutaneousintramuscular, and intradermal administrations. In some embodiments,parenteral administration of the compositions includes direct tissueinjections. Preparations for parenteral administration include sterilesolutions ready for injection, sterile dry soluble products, such aslyophilized powders, ready to be combined with a solvent or sterilesolution just prior to use, including hypodermic tablets, sterilesuspensions ready for injection, sterile dry insoluble products ready tobe combined with a vehicle just prior to use and sterile emulsions. Insome embodiments, the solutions can be either aqueous or nonaqueous.

Pharmaceutically acceptable carriers used in parenteral preparationsinclude aqueous vehicles, nonaqueous vehicles, antimicrobial agents,isotonic agents, buffers, antioxidants, local anesthetics, suspendingand dispersing agents, emulsifying agents, sequestering or chelatingagents and other pharmaceutically acceptable substances.

Examples of aqueous vehicles include Sodium Chloride Injection, RingersInjection, Isotonic Dextrose Injection, Sterile Water Injection,Dextrose and Lactated Ringers Injection. Nonaqueous parenteral vehiclesinclude fixed oils of vegetable origin, cottonseed oil, corn oil, sesameoil and peanut oil. Antimicrobial agents in bacteriostatic orfungistatic concentrations must be added to parenteral preparationspackaged in multiple-dose containers which include phenols or cresols,mercurials, benzyl alcohol, chlorobutanol, methyl and propylp-hydroxybenzoic acid esters, thiomersal, benzalkonium chloride andbenzethonium chloride. Isotonic agents include sodium chloride anddextrose. Buffers include phosphate and citrate. Antioxidants includesodium bisulfate. Local anesthetics include procaine hydrochloride.Suspending and dispersing agents include sodium carboxymethylcelluose,hydroxypropyl methylcellulose and polyvinylpyrrolidone. Emulsifyingagents include Polysorbate 80 (TWEEN® 80). A sequestering or chelatingagent of metal ions includes EDTA. Pharmaceutical carriers also includeethyl alcohol, polyethylene glycol and propylene glycol for watermiscible vehicles and sodium hydroxide, hydrochloric acid, citric acidor lactic acid for pH adjustment.

The concentration of the IL-10 can be adjusted so that administration,e.g., an injection or infusion, provides an effective amount to producethe desired pharmacological effect. The exact dose depends on the age,weight and condition of the patient or animal as is known in the art.

The unit-dose parenteral preparations can be packaged in container, forexample, an ampoule, a vial or a syringe with a needle. All preparationsfor parenteral administration must be sterile, as is known and practicedin the art.

Illustratively, subcutaneous infusion of a sterile aqueous solutioncontaining an active compound is an effective mode of administration.Another embodiment is a sterile aqueous or oily solution or suspensioncontaining an active material injected as necessary to produce thedesired pharmacological effect.

Injectables are typically designed for local administration. Typically atherapeutically effective dosage is formulated to contain aconcentration of at least about 0.01% ww up to about 4% ww or more,preferably more than 0.1% ww of the active compound to the treatedtissue(s). It is to be further understood that for any particularsubject, specific dosage regimens should be adjusted over time accordingto the individual need and the professional judgment of the personadministering or supervising the administration of the formulations, andthat the concentration ranges set forth herein are exemplary only andare not intended to limit the scope or practice of the claimedformulations.

The compositions provided herein can be formulated for parenteraladministration, e.g., by bolus administration or continuous infusion.Formulations for administration can be presented in unit dosage form,e.g., in ampoules or in multi-dose containers, optionally with an addedpreservative. The compositions can be suspensions, solutions oremulsions in oily or aqueous vehicles, and can contain formulatoryagents such as suspending, stabilizing and/or dispersing agents.Alternatively, the active ingredient can be in powder form forreconstitution with a suitable vehicle, e.g., sterile pyrogen-free wateror other solvents, before use.

Some embodiments also include pharmaceutical formulations for parenteraladministration, e.g., by bolus administration or continuous infusion,include aqueous suspensions of a hydrogel, having encapsulated thereinIL-10. Additionally, suspensions of the hydrogel may be prepared asappropriate. Formulations for administration may be presented in unitdosage form, e.g., in ampoules or in multi-dose containers, with anadded preservative. The formulations may take such forms as suspensions,solutions or emulsions in oily or aqueous vehicles, and may containformulatory agents such as suspending, stabilizing and/or dispersingagents. In some embodiments the formulation can be administered bysubcutaneous injection.

The effective daily dosage of the therapeutic agent may be varied over awide range; e.g., from about 0.05 pg to about 10,000 ng per adult humanper day.

Some embodiments provide a method of administering IL-10 to a subject,once about every 5, 10, 12, 15, 20 or 24 hrs. In some embodiments, theIL-10 is administered to a subject at least 1, 2, 3, 4, 5, 6, 8, or 12times daily.

Methods of Treatment

Some embodiments relate to a method for treating a wound with anextended release biocompatible composition as disclosed and describedherein. In some embodiments, the composition may be a hydrogel.

In some embodiments, the wound may be formed by an incision during asurgical procedure. In some embodiments, the wound can be caused by aclean, sharp-edged object such as a knife, scalpel or a razor.

In some embodiments, the wound can be an open type trauma wound. In someaspects, the open type trauma wound can be a severe trauma wound; forexample, gunshot wounds, improvised explosive device (IED) wounds,mortar attack wounds, missile attack wounds, rocket propelled grenade(RPG) wounds, grenade wounds, bomb wounds, land mind wounds, and anymilitary or improvised ordinance wounds.

In some embodiments, the wound can be contacted with the extendedrelease biocompatible composition and a dressing. In some aspects, thedressing can be bound to the skin, forming a barrier to prevent furtherbleeding or oozing of bodily fluids. In some aspects, the dressing canbe a surgical dressing. In some aspects, the dressing can be a fieldwound dressing.

In some embodiments, the wound may be torn, cut or punctured skin.

In some embodiments, the wound may be a penetrating wound. Penetratingwounds can be classified into a number of different types, according tothe object that caused the wound. The types of penetrating wounds thatcan be treated with the present formulations can include, but are notlimited to,

-   -   Incisions or incised wounds—caused by a clean, sharp-edged        object such as a knife, scalpel, a razor or a glass splinter;    -   Lacerations—irregular wounds caused by a blunt impact to soft        tissue which lies over hard tissue (e.g. laceration of the skin        covering the skull) or tearing of skin and other tissues;    -   Puncture wounds—caused by an object puncturing the skin, such as        a nail, knife, or bullet.    -   Gunshot wounds—caused by a bullet or similar projectile driving        into or through the body. There may be two wounds, one at the        site of entry and one at the site of exit;    -   Improvised explosive device (IED) wounds—caused by an object        from a IED or propelled by a IED driving into or through the        body. There may be two wounds, one at the site of entry and one        at the site of exit;    -   Mortar attack wounds—caused by an object from a mortar or        propelled by a mortar driving into or through the body. There        may be two wounds, one at the site of entry and one at the site        of exit;    -   Missile attack wounds—caused by an object from a missile or        propelled by a missile driving into or through the body. There        may be two wounds, one at the site of entry and one at the site        of exit;    -   Rocket propelled grenade (RPG) wounds—caused by an object from a        RPG or propelled by a RPG driving into or through the body.        There may be two wounds, one at the site of entry and one at the        site of exit;    -   Grenade wounds—caused by an object from a grenade or propelled        by a grenade driving into or through the body. There may be two        wounds, one at the site of entry and one at the site of exit;    -   Bomb wounds—caused by an object from a bomb or propelled by a        bomb driving into or through the body. There may be two wounds,        one at the site of entry and one at the site of exit;    -   Land mind wounds—caused by an object from a land mind or        propelled by a land mind driving into or through the body. There        may be two wounds, one at the site of entry and one at the site        of exit;    -   Any military or improvised ordinance wounds—caused by an object        from any military or improvised ordinance or propelled by any        military or improvised ordinance driving into or through the        body. There may be two wounds, one at the site of entry and one        at the site of exit.

Non-penetrating wounds can be classified into a number of differenttypes. The types of non-penetrating wounds that can be treated with thepresent formulations can include, but are not limited to,

-   -   First-degree abrasions involving only epidermal injury;    -   Second-degree abrasions involving the epidermis as well as the        dermis;    -   Third-degree abrasions involving damage to the subcutaneous        layer and the skin;    -   First-degree burns involving only epidermal injury    -   Second-degree burns involving the epidermis as well as the        dermis;    -   Third-degree burns involving damage to all layers of the skin;    -   Fourth-degree burn involving damage to all layers of the skin        and deeper tissues; and    -   Skin grafts.

The burns can be classified into a number of different types, accordingto the object that caused the wound. For example, the burn can be athermal burn, chemical burn, electrical burn, or radiation burn. In someembodiments, the composition including IL-10 may be a gel, lotion, creamor ointment that may be applied to a burn area. In some embodiments, thecomposition including IL-10 may be a gel, lotion, cream or ointmentincluding a hydrogel that may be applied to the burn area.

In some embodiments, the prevention or reduction of scarring afforded byan extended release biocompatible composition encompasses any reductionin scarring as compared to the level of typically observed for a similarwound that is not treated with the extended release biocompatiblecomposition. In some embodiments, the prevention or reduction ofscarring afforded by an extended release biocompatible compositionincluding IL-10 encompasses any reduction in scarring as compared to thelevel of typically observed for a similar wound that is treated withIL-10 without extended release properties.

In some embodiments, the extended release biocompatible composition mayprevent or reduce scarring in the intraabdominal cavity, kidney, lung,or liver. In some embodiments, the extended release biocompatiblecomposition may prevent or reduce scarring in the dermal layer orepidermis. In some embodiments, the extended release biocompatiblecomposition may be used to accelerate healing and reduce scarring of theskin.

In considering the macroscopic appearance of a scar resulting from atreated wound, the extent of scarring, and hence the magnitude of anyreduction in scarring achieved, may be assessed with reference to any ofa number of parameters.

Suitable parameters for the macroscopic assessment of scars may include,but are not limited to, color of the scar; height of the scar; surfacetexture of the scar; and stiffness of the scar. Additional parametersfor assessment of scars may include, but are not limited to, weaveappearance of the collagen in the dermis, reconstitution of dermalappendages, number and appearance of sebaceous glands, and number andappearance of hair or hair follicles.

Some embodiments provide a composition and method for wound healingwhere the wound area has features of normal skin after treatment of awound with the composition. In some embodiments, the features may beaesthetic appearance of the skin surface, barrier function, or tensilestrength. In some embodiments, the features may be that all layerspresent in normal epidermis are present in the epidermis of the treatedwound where in a scar not all layers of the epidermis are typicallypresent.

In some embodiments, the features may be dermal appendages that arefound in normal skin but are not typically found in a wound area thathas not been treated. Typically dermal appendages are significantlyreduced in a scar area. In some embodiments, the dermal appendages maybe hair, hair follicles, arrector pilli, sebaceous glands or sweatglands. In some embodiments, the dermal appendages may be hair and hairfollicles. In some embodiments, the dermal appendages may be sebaceousglands or sweat glands.

In some embodiments, the wound may be the result of a thermal burn,chemical burn, electrical burn, or radiation burn. In some embodiments,the composition may be a gel, lotion, cream or ointment that may beapplied to a burn area.

In some embodiments, the composition includes IL-10. In someembodiments, the morphology of the epidermal surface of the wound areaafter treatment is similar to the morphology of the epidermal surface ofnormal skin. In some embodiments, the epidermal height of the wound areaafter treatment with the composition is similar to the epidermal heightof normal skin. In some embodiments, the orientation of the nucleus ofthe basal keratinocytes of the wound area after treatment with thecomposition is similar to the orientation of the nucleus of the basalkeratinocytes of normal skin.

In some embodiments, the composition may be an extended releasebiocompatible composition including a biodegradable support scaffold;and IL-10. In some embodiments, the amount of IL-10 in the compositionis from about 0.2 μM to about 2.5 μM. In some embodiments, thecomposition is administered in a single dosage and provides features ofnormal skin after treatment of a wound in a wound area after a period oftime. In some embodiments, the features in the wound area are evaluatedusing an Assessment Scale value to obtain an Assessment Scale score. Insome embodiments, the biodegradable support scaffold compriseshyaluronan or a hyaluronan moiety. In some embodiments, the hyaluronanis hyaluronic acid. In some embodiments, the biodegradable supportscaffold comprises a heparin or heparan sulfate. In some embodiments,the biodegradable support scaffold comprises collagen. In someembodiments, the collagen is human collagen. In some embodiments, thecollagen is Type-I collagen. In some embodiments, the collagen isType-III collagen. In some embodiments, the collagen is Type-I collagen,Type-II collagen or Type-III collagen, or any combination thereof. Insome embodiments, the biodegradable support scaffold comprises PEG or aPEG moiety. In some embodiments, the extended release biocompatiblecomposition including a biodegradable support scaffold; and IL-10 andmethod for wound healing provides features of normal skin aftertreatment of a wound that is improved compared to a composition thatincludes biodegradable support scaffold without IL-10. In someembodiments, the extended release biocompatible composition including abiodegradable support scaffold and IL-10, and the method for woundhealing using such composition, restores dermal appendages at a levelgreater than the dermal appendages restored in scar formation withouttreatment or in wound treatment with a composition that does not includeIL-10. In some embodiments, a wound will heal to have dermal appendagesto the level of generally observed for normal skin. In some embodiments,a wound will heal to restore at least two dermal appendages to a levelof 50% or greater than generally observed for normal skin as assessedwith reference to at least two of the parameters set out herein orotherwise known in the art.

In some embodiments, the biodegradable support scaffold providesbeneficial effects without IL-10 and the IL-10 provides beneficialeffects without the biodegradable support scaffold and a compositionincluding both a biodegradable support scaffold and IL-10 has a greaterbeneficial effect than would be achieved by separate treatment of thewound with biodegradable support scaffold and IL-10. In someembodiments, the biodegradable support scaffold provides beneficialeffects without IL-10 and the IL-10 provides beneficial effects withoutthe biodegradable support scaffold and a composition including both abiodegradable support scaffold and IL-10 has a greater beneficial effectthan would be achieved by separate treatment of the wound withbiodegradable support scaffold and IL-10 using a mouse model to evaluatethe beneficial effect. In some embodiments, the beneficial effect of thecomposition including both a biodegradable support scaffold and IL-10 is10% or greater, 20% or greater, 30% or greater, 40% or greater, 50% orgreater, 60% or greater, 70% or greater or 80% or greater than would beachieved by separate treatment of the wound with biodegradable supportscaffold and IL-10. In some embodiments, the beneficial effect of thecomposition including both a biodegradable support scaffold and IL-10 is10% or greater, 20% or greater, 30% or greater, 40% or greater, 50% orgreater, 60% or greater, 70% or greater or 80% or greater than would beachieved by separate treatment of the wound with biodegradable supportscaffold and IL-10 using a mouse model to evaluate the beneficialeffect. In some embodiments, the beneficial effect of the compositionincluding both a biodegradable support scaffold and IL-10 is 10% orgreater, 20% or greater, 30% or greater, 40% or greater, 50% or greater,60% or greater, 70% or greater or 80% or greater than would be achievedby treatment of the wound with biodegradable support scaffold and noIL-10. In some embodiments, the beneficial effect of the compositionincluding both a biodegradable support scaffold and IL-10 is 10% orgreater, 20% or greater, 30% or greater, 40% or greater, 50% or greater,60% or greater, 70% or greater or 80% or greater than would be achievedby treatment of the wound with biodegradable support scaffold and noIL-10 using a mouse model to evaluate the beneficial effect. In someembodiments, the beneficial effect of the composition including both abiodegradable support scaffold and IL-10 is 10% or greater, 20% orgreater, 30% or greater, 40% or greater, 50% or greater, 60% or greater,70% or greater or 80% or greater than would be achieved by treatment ofthe wound with IL-10 and no biodegradable support scaffold. In someembodiments, the beneficial effect of the composition including both abiodegradable support scaffold and IL-10 is 10% or greater, 20% orgreater, 30% or greater, 40% or greater, 50% or greater, 60% or greater,70% or greater or 80% or greater than would be achieved by treatment ofthe wound with IL-10 and no biodegradable support scaffold using a mousemodel to evaluate the beneficial effect. In some embodiments, thebeneficial effect of the composition including both a biodegradablesupport scaffold and IL-10 is 10% or greater, 20% or greater, 30% orgreater, 40% or greater, 50% or greater, 60% or greater, 70% or greateror 80% or greater than would be achieved by separate treatment of thewound with biodegradable support scaffold and IL-10. In someembodiments, the beneficial effect may be aesthetic appearance of theskin surface, barrier function, tensile strength, or a combinationthereof. In some embodiments, the beneficial effect may be that alllayers present in a normal epidermis are present in the treatedepidermis where in a scar not all layers present in a normal epidermisare typically present. In some embodiments, the beneficial effect may bethe treated wound area having dermal appendages at a level closer tonormal skin than the dermal appendages present in a wound area that hasnot been treated or that has not been treated with the compositions andmethods provided herein. In some embodiments, the beneficial effect maybe hair, hair follicles, arrector pilli, sebaceous glands or sweatglands in the wound area that are found in normal skin but are nottypically found, or are found in reduced levels compared to a wound areathat has not been treated or that has not been treated with thecompositions and methods provided herein. In some embodiments, thedermal appendages may be hair and hair follicles. In some embodiments,the dermal appendages may be sebaceous glands or sweat glands.

In some embodiments, the parameters can be evaluated using an AssessmentScale where an Assessment Scale value (INDEX) is obtained. In someembodiments, the Assessment Scale value (INDEX) for each parameter maybe used to obtain an Assessment Scale Score where the Assessment ScaleScore=(^(n)Σ INDEX/n)×100 where n is the number of parameters beingevaluated and a score of 100 would be a scar that is indistinguishablefrom normal skin (or un-injured skin). In some embodiments, n may be 2,3 4, 5 or 6. In some embodiments, a score of greater than 50 shows animprovement over normal scarring. In some embodiments, at least oneepidermal and at least one dermal parameter may be evaluated. In someembodiments, the scar is evaluated in a mouse model. In someembodiments, the mice used in the mouse model are C57B16J mice. In someembodiments, the scar is evaluated on day 28 after wounding. In someembodiments, the wounds are harvested at 30 and 90 days and assessed.

In some embodiments, the wound treatment result provides an AssessmentScale score of 50 to 80. In some embodiments, the Assessment Scale scoremay be 50 to 70. In some embodiments, the Assessment Scale score may be50 to 60. In some embodiments, the Assessment Scale score may be about50. In some embodiments, the Assessment Scale score may be 80 to 130. Insome embodiments, the Assessment Scale score may be 90 to 120. In someembodiments, the Assessment Scale score may be 100 to 110. In someembodiments, the Assessment Scale score may be up to 200

In some embodiments, a wound will heal to have less scarring compared tothe level of generally observed for a similar wound that is not treatedwith the extended release biocompatible composition and will demonstratea reduction in scarring as assessed with reference to at least one ofthe parameters for macroscopic assessment set out herein or otherwiseknown in the art. In some embodiments, a wound will heal to have lessscarring compared to the level of generally observed for a similar woundthat is not treated with the extended release biocompatible compositionand will demonstrate a reduction in scarring as assessed with referenceto at least two of the parameters for macroscopic assessment set outherein or otherwise known in the art. In some embodiments, a wound willheal to have less scarring compared to the level of generally observedfor a similar wound that is not treated with the extended releasebiocompatible composition and will demonstrate a reduction in scarringas assessed with reference to at least three of the parameters formacroscopic assessment set out herein or otherwise known in the art. Insome embodiments, a wound will heal to have less scarring compared tothe level of generally observed for a similar wound that is not treatedwith the extended release biocompatible composition and will demonstratea reduction in scarring as assessed with reference to all of theparameters for macroscopic assessment set out herein or otherwise knownin the art.

Suitable parameters for the microscopic assessment of scars may include,but are not limited to, thickness of extracellular matrix fibers;orientation of extracellular matrix fibers; extracellular matrix fiberscomposition of the scar; and cellularity of the scar.

In some embodiments, a wound will heal to have less scarring compared tothe level of generally observed for a similar wound that is not treatedwith the extended release biocompatible composition and will demonstratea reduction in scarring as assessed with reference to at least one ofthe parameters for microscopic assessment set out herein or otherwiseknown in the art. In some embodiments, a wound will heal to have lessscarring compared to the level of generally observed for a similar woundthat is not treated with the extended release biocompatible compositionand will demonstrate a reduction in scarring as assessed with referenceto at least two of the parameters for microscopic assessment set outherein or otherwise known in the art. In some embodiments, a wound willheal to have less scarring compared to the level of generally observedfor a similar wound that is not treated with the extended releasebiocompatible composition and will demonstrate a reduction in scarringas assessed with reference to at least three of the parameters formicroscopic assessment set out herein or otherwise known in the art. Insome embodiments, a wound will heal to have less scarring compared tothe level of generally observed for a similar wound that is not treatedwith the extended release biocompatible composition and will demonstratea reduction in scarring as assessed with reference to all of theparameters for microscopic assessment set out herein or otherwise knownin the art.

While not wishing to be bound by the following, it is believed that theextended release biocompatible compositions as disclosed and describedherein provide wound healing properties beyond those of any heretoforeused formulations by virtue of the sustained release of IL-10 in thepresent compositions. Single injection of an extended releasebiocompatible composition including IL-10 provides superior woundhealing properties in comparison to single injection of IL-10 notincluded in an extended release formulation. In addition, it is believedthat, by providing both the ability to initiate the wound healingresponse and to sustain the wound healing response, the compositions andmethods provided herein provide particular advantages over presentcompositions. Further, it is believed that the hyaluronan-containingbiocompatible compositions as disclosed and described herein providewound healing properties beyond those of any heretofore usedformulations by virtue of the synergistic effect provided by thecombination of hyaluronan IL-10. Single injection of extended releasebiocompatible composition including IL-10 and hyaluronan providessuperior wound healing properties in comparison to single injection ofIL-10 without hyaluronan.

Suitable parameters for the clinical measurement and assessment of scarsmay be selected based upon a variety of measures or assessmentsincluding those described by Beausang et al. (A new quantitative scalefor clinical scar assessment. Plast Reconstr Surg., 1998, 102:1954-1961) and van Zuijlen et al. (Scar assessment tools: implicationsfor current research. Plast Reconstr Surg., 2002, 109(3): 1108-1122).For example, suitable parameters include, but are not limited to,assessment with regard to Visual Analogue Scale (Vas) Scar Score; scarheight, scar width, scar perimeter, scar area or scar volume; appearanceand/or color of scar compared to surrounding unscarred skin; scardistortion and mechanical performance; and scar contour and scartexture.

In some embodiments, the extended release biocompatible composition maybe administered to a wound site that provides a first amount of IL-10 atthe wound site during a first time period and provides a second amountof IL-10 at the wound site during a second time period.

Some embodiments relate to an extended release biocompatible compositionthat upon administration can result in a maximum concentration (Tmax) atthe wound site during a bolus time period measured from initialadministration of composition. In some embodiments, the extended releasebiocompatible composition upon administration can result in a Tmax ofIL-10 from about 0.05 ng/mL to about 10000 ng/mL to the tissue at thewound site during the bolus time period measured from initialadministration of composition.

It is understood that during the administration period the wound mayheal and no longer actually be considered to be a wound.

In any of the embodiments disclosed and described herein, IL-10 relatedpeptides disclosed in US. Publication No. 2008/0139478 may be includedin the compositions and methods in place of IL-10. For example, SEQ. ID1 or SEQ. ID 2 disclosed in US. Publication No. 2008/0139478 may beincluded in the compositions and methods in place of IL-10.

In any of the embodiments disclosed and described herein, a fragment orpartially modified form of IL-10 disclosed in U.S. Pat. No. 7,052,684may be included in the compositions and methods in place of IL-10. Forexample, a fragment or partially modified form of IL-10 may have atleast 40% homology with IL-10. In some embodiments, the fragment orpartially modified form of IL-10 may have at least 50, 60, 70, 80, 90 or95% homology with IL-10.

EXAMPLES Example 1 Preparation of Extended Release BiocompatibleComposition

Composition 1 is prepared by mixing high molecular weight hyaluronan(HA), heparin sulfate and rIL-10 to prepare a mixture. The mixture iscombined with PEG diacrylate and Type I collagen. Subsequently, the HAis chemically cross-linked with PEG diacrylate forming a stable matrix.Type I collagen may improve the gel quality for in vitro experiments.

It was determined that a ratio of 2:1:1 (HA:Collagen: cross-linker)results in sustained release of rIL-10 in vitro for seven days. FIG. 1Ashows HH10 (purple line) in vitro can result to sustained delivery ofIL-10 for 7 days. To evaluate the biologic activity of the releasedrIL-10 from the composition, its ability to induce HA rich pericellularmatrix (PCM) formation by postnatal dermal fibroblasts was assessed. Totest the biologic activity of the rIL10 released by composition 1, gels(25 μL loaded with 800 ng of rIL-10) were placed in cell culture wellsin media (250 μL, Dulbecco's Modified Eagle Medium, Life TechnologiesCorporation, Carlsbad, Calif.), which was changed daily. The conditionedmedia from each daily change was then added to postnatal dermalfibroblasts in cell culture which resulted in the formation of large HArich pericellular matrices formed by the dermal fibroblasts for up toseven days demonstrating the intact biologic activity of the rIL-10released by HH10. FIG. 1B shows IL-10 released from HH10 induces largeHA rich PCM by adult fibroblasts for up to 7 days.

Example 2 Evaluation of Composition 1

Composition 1 induces skin regeneration and prevents wound scaring inmice. FIG. 2A shows HH10 results in wound healing that isindistinguishable from the surrounding skin. FIG. 2B shows rIL-10 alsoattenuates scar formation to a much lesser degree; both compared to PBStreated wounds (FIG. 2C). The black arrows mark the area of the residualwound HH10 reduces scar area (FIG. 2D) and increases the number ofdermal appendages (FIG. 2E) at 30 days compared to both rIL-10 or PBScontrol with skin integrity, (tensile strength) that is statistically nodifferent than unwounded skin (FIG. 2F). For example, administration ofa single dose of Composition 1 (loaded with 800 ng/mL of IL-10) resultsin a regenerative wound repair at 30 (FIG. 2A) and 90 days compared toboth PBS (FIG. 2B) control treated wounds and wounds treated with asingle dose of recombinant IL-10 (200 ng) (FIG. 2C) in C57B16J mice.Wound treated with Composition 1 (FIG. 2A) have similar basket weaveappearance of the collagen in the dermis, reconstitution of dermalappendages and a normal appearing epidermis to uninjured skin. Treatmentwith Composition 1 results in a significant reduction of scar area at 30days compared to controls and significant increase in dermal appendages(hair follicles) to levels not significantly different to unwounded skin(FIG. 2D-E). Similarly, IL-10 results in wound healing with similarbiomechanical properties compared to unwounded skin, including tensilestrength (FIG. 2F), stiffness and modulus.

Example 3 Murine Excisional Wound Healing Model I

A murine excisional wound healing model is used to evaluate Composition1 C57BL/6j mice are shaved and prepared; two 4 mm full thickness woundsare created using a dermal punch biopsy on the flanks. These wounds arelabeled with India ink and a sterile transparent dressing are placedover the wound. Twenty-five microliters of Composition 1 or controltreatments are injected into the wound well. In a separate group ofanimals, a silicone stent of 6-mm inner diameter is secured around thewounds using instant Krazy glue and interrupted 6-O nylon sutures tocontrol for contracture in loose skinned murine wounds. Animals arehoused individually.

Forty mice having bilateral wounds created with and without the siliconestents to control for contracture are evaluated. Wounds are harvested at30 and 90 days and assessed for regenerative healing.

Tissue Handling Processing:

At 30 and 90 days post wounding, mice are shaved and the wound site isidentified by the India ink staining. Wound is harvested and thenbisected in a vertical axis to maintain consistent wound orientation forscar analysis. Wounds are fixed overnight in 10% neutral bufferedformalin, processed and paraffin embedded. 5 μm sections are collectedand stained with H&E and Masson's trichrome to analyze wound repairoutcomes.

Regenerative Wound Healing Analysis:

To assess regenerative wound healing, both H&E and trichrome sectionsare analyzed by the following parameters: 1) scar width, height and areaas calculated with computer assisted morphometry, 2) evaluation of theepidermis by epidermal height and epidermal flatness, and 3)quantification of dermal appendages. Each of these wound repairparameters are given a numeric score. These scores are fitted using theMinitab software, and the data is extrapolated to predict the optimalformulation of Composition 1 that will yield maximal wound healingefficacy.

Biomechanical Testing:

To assess wound/skin integrity, tensile testing is performed. 35 mm×6mm-templated rectangular skin samples with wounds in the middle inbetween intact skin segments are harvested after 30 and 90 days. Theedges are placed in custom grips attached to an electromechanicaltesting system with a 10 Newton (N) load cell. Apparent wound stiffnessis determined as the slope (in N/m) of the load-elongation curve in thelinear region, and the maximum tensile force before wound failure isrecorded (FIG. 2B).

Example 4 Murine Excisional Wound Healing Model II

A murine excisional wound healing model is used to evaluate toxicologyof Composition 1. Two 4 mm full thickness wounds are prepared using adermal punch biopsy on the flanks into 30 C57b1/6j mice. Mice (10/group)are treated without Composition 1 (control) or Composition 1 at aselected dosage administered once on day 0, or daily to the same woundfor 10 straight days. Five animals per group are sacrificed on day 10and on day 17, allowing for a 7-day recovery phase for each group.

Gross Observations.

Gross observations as a measurement of drug safety are conducted dailythroughout the study and include the following: respiration, posture,activity, pallor, and weight.

Hemotology.

Hematology is performed on serum samples collected at 0, 48 hr, day 7and day 14. Hematology readouts include: leukocyte count, erythrocytecount, hemoglobin, hematocrit, MCH, MCV, MCHC, platelet count,differential count, cellular morphology, and reticulocyte count.

Biochemistry.

Clinical chemistry readouts include: alkaline phosphatase, ALT, AST, CK,albumin, total protein, globulin, total bilirubin, direct bilirubin,indirect bilirubin, BUN, creatinine, cholesterol, glucose, calcium,phosphorus, TCO₂, chloride, potassium, sodium, NA/K ratio, A/G ratio andB/C ratio.

Histopathology.

Histopathological examination is performed on the following selectedtissues at the end of in-life of the study: skin, liver, kidney, lung,heart, spleen, and pancreas. Tissues are fixed in 10% neutral bufferedformalin, embedded in paraffin and stained with hematoxylin and eosinstains. Samples are evaluated by light microscopy and scored by a StudyPathologist using standard methods.

A total of 30 C57b1/6j wild-type mice are used to complete the studytaking up to 3 months for completion.

Example 5 rhIL-10 Binding/Release Kinetics Assay

Composition 1 is solidified with between 1.0 to 40 ug/ml of rhIL-10 in48-well plates for 1 hour at room temperature. Composition 1 is washedone time with 250 μL of PBS-BSA to remove any unbound rhIL-10. The totalamount of unbound rhIL-10 collected in the PBS-BSA wash for each well isdetermined using ELISA. After the PBS-BSA wash, each well receives 250uL of fresh PBS-BSA. The plates are incubated at 37° F. degrees for 14days. Starting on day 0, and every 2 days up to 14 days, 100 μL ofsupernatant is removed from a new set of triplicate wells, and analyzedfor the amount of free rhIL-10. The level of free rhIL-10 in the PBS-BSAat day 0 acts as the baseline control. In addition, negative controlwells consisting of the same hydrogel formulation included inComposition 1, but without rhIL-10, will act as the daily controls.

Example 6 rhIL-10 Potency Assay

Composition 1 is cultured in 48-well tissue culture plates at 37° F. for14 days. Supernatants (100 μL) from the Composition 1 culture wells areharvested on days 0, 7 and 14. The concentration of rhIL-10 in thesupernatants will be determined using ELISA. The biological activity ofthe rhIL-10 release from Composition 1 is determined by measuring theproliferative response of MC9 cells (ATCC # CRL-8306). MC9 cells are amouse mast cell line that proliferates in response to rhIL-10 in thepresence of IL-4. This cell line is commonly used to quantify rhIL-10potency. A typical EC₅₀ of fully active hIL-10 is expected to be in therange of 0.1 to 1 ng/mL. The assay provides biological activity ofrhIL-10 released from Composition 1 may be equal to the biologicalactivity of rhIL-10 prior to inclusion in Composition 1. MC9proliferation is measured using a colorimetric dye reduction assay (MTT,Sigma) in a 96 well format.

Example 7 Extended Release Biocompatible Composition 2

Composition 2 is prepared in a similar manner to that described inExample 1 where the amount of IL-10 in the composition is from about 0.2μM to about 2.5 μM.

Example 8 Evaluation of Composition 2

The effect of Composition 2 (which includes IL-10) on wound healing hasbeen compared to the extended release biocompatible composition withoutIL-10. Several dermal and epidermal parameters have been studied toidentify the effect of scaffold only (gel control) vs. extended releasebiocompatible composition (Composition 2) on cutaneous wound repair. Theparameters include the quantification of epidermal height and thenuclear orientation of the basal keratinocytes in the epidermis; and thequantification of the scar area, dermal appendages and vessel density inthe dermis of the wounds. The data is compared to unwounded skin,characteristic scar and regenerative wound healing observed in woundstreated with lentiviral overexpression of IL-10 at the wound site.

The differences between murine uninjured skin and a scar arehistologically very distinct. Murine skin has 2 major layers, theepidermis and the dermis. Several quantifiable parameters wereidentified in the epidermis as well as in the dermis that can be used toevaluate the differences in the extent of scarring in murine cutaneouswounds. The parameters include i) the quantification of topography, ii)epidermal height, and iii) the nuclear orientation of the basalkeratinocytes in the epidermis; and iv) the quantification of the scararea, v) dermal appendages, and vi) vascularity (vessel density) in thedermis of the scars. Each of these parameters is measured in the central12 portion of the scar being evaluated.

The wound samples are harvested with the wound in the middle surroundedby intact uninjured skin. The entire wound/scar is divided into 4quarters and the central 12 portion of the scar is evaluated for thedifferent dermal and epidermal parameters.

Epidermal Parameters

Topographical score: This is based on the morphology or the undulationpattern of the epidermal surface. Histologically the surface of theuninjured skin has more undulations as compared to the scar which givesthe scar its characteristic flat appearance. The epidermal length ismeasured per 200 μm of grid length (measured in 3-6 200 μm fields persample).

Epidermal Height:

The epidermal height is measured as the height from epidermal-dermaljunction to top of the epidermis. Epidermal height is usually more inthe area of the scars as compared to the skin, and it is measured in μm(3 measurements per 200 μm grid).

Orientation of the Nucleus of the Basal Keratinocytes:

The polarity of the epidermal cell, is measured in terms of Sin θ, whereθ is the angle between the line through the long axis of the nucleus ofthe basal cell and the epidermal-dermal junction. The maximum value isone. In case of skin, the cells being more columnar in shape andoriented perpendicular to the epidermal-dermal junction, Sin θ is closerto one, and in scars, the cells being more flattened and parallel to theepidermal-dermal junction, have a value less than one.

Dermal Parameters

Scar Area:

Histologic wound sections are scanned from edge to edge. Computerassisted morphometric image analysis is used to measure the total scararea (measured in square micrometers) per each wound section.

Dermal Appendages:

Adnexal structures including hair follicles, sabaceous (oil) glands andsweat glands are observed in uninjured skin. Dermal appendages aresignificantly reduced in scars as compared to uninjured skin. The numberof dermal appendages per 200 μm grid (measured in 3-6 200 μm fields persample) is measured and compared to uninjured skin.

Vascular Density:

Vascularity is less in the scar compared to the normal uninjured skin.The number of CD31-positive lumens per 200 μm grid (measured in 3-6 200μm fields per section) is measured.

The parameters can be evaluated using an Assessment Scale where theparameters in the treated area may be compared to parameters in a normalskin area and/or parameters in an untreated scar area after a period oftime. For each parameter an Assessment Scale value (INDEX) may beobtained. In some embodiments, INDEX=[(treated wound areaparameter-untreated wound area parameter)/(non-wounded areaparameter-untreated wound area parameter)] or mathematical equivalentthereof. In some embodiments, the treated area may be histologicallycloser in at least two parameters to normal skin than it is to untreatedscar area. In some embodiments, the Assessment Scale value of two ormore parameters may be used to calculate an Assessment Scale score. Insome embodiments, the Assessment Scale Score=(^(n)Σ INDEX/n)×100 where nis the number of parameters being evaluated and a score of 100 would bea treatment result that provides a “scar” that is indistinguishable fromnormal skin (or un-injured skin). In some embodiments, n may be 2, 3 4,5 or 6. In some embodiments, a score of greater than 50 shows animprovement over normal scarring. In some embodiments, the woundtreatment result provides a score of greater than 60. In someembodiments, the wound treatment result provides a score of greater than70. In some embodiments, the wound treatment result provides a score ofgreater than 80. In some embodiments, the wound treatment resultprovides a score of greater than 90. In some embodiments, the score isabout 50, 60, 70, 80, 90, 100, 110, 120, 130 or 200, or within a rangedefined by any two of the preceding values. In some embodiments, atleast one epidermal and at least one dermal parameter may be evaluated.In some embodiments, the scar is evaluated in a mouse model. In someembodiments, the mice used in the mouse model are C57B1/6J mice. In someembodiments, the scar is evaluated on day 28 after wounding. In someembodiments, the wounds are harvested at 30 and 90 days and assessed.

In some embodiments, the non-wounded area parameter is a standardparameter value for age of patient. In some embodiments, the age of thepatient may be from about 1 day old to about 10 days old. In someembodiments, the age of the patient may be from about 10 days old toabout 1 month old. In some embodiments, the age of the patient may befrom about 1 month old to about six months old. In some embodiments, theage of the patient may be from about six months old to about 1 year old.In some embodiments, the age of the patient may be from about 1 year oldto about 2 years old. In some embodiments, the age of the patient may befrom about 2 years old to about 6 years old. In some embodiments, theage of the patient may be from about 6 years old to about 16 years old.In some embodiments, the age of the patient may be from about 16 yearsold to about 26 years old. In some embodiments, the age of the patientmay be from about 26 years old to about 36 years old. In someembodiments, the age of the patient may be from about 36 years old toabout 56 years old. In some embodiments, the age of the patient may befrom about 56 years old to about 76 years old. In some embodiments, theage of the patient may be from about 76 years old to about 96 years oldor greater. In some embodiments, the treatment result provides a scoreof greater than 60. In some embodiments, a score of greater than 70. Insome embodiments, a score of greater than 80. In some embodiments, ascore of greater than 90. In some embodiments, the score is about 50,60, 70, 80, 90, 100, 110, 120, 130 or 200, or within a range defined byany two of the preceding values.

Evaluation of Wounded Skin

The treatment of wounds using gel only (control), HH-10 (Composition 2)and wounds treated with lentiviral over expression of IL-10 (LV IL-10)were compared to each other and unwounded skin and wounded skin that wasuntreated (scar) at day 28 post wounding. Several epidermal parametersand dermal parameters were evaluated. FIGS. 3A-B show quantification ofepidermal height and the nuclear orientation of the basal keratinocytesin the epidermis of the wounds, and FIGS. 3C-E show quantification ofscar area, dermal appendages and vessel density in the dermis of thewounds where the different treatments and controls are listed along theX-axis. Treatment with Composition 2 (HH10) results in significantlyimproved wound healing based on the observed parameters compared to gelonly (control). Composition 2 (HH10) treated wound at day 28 postwounding, and gel control treated wound at day 28 post wounding werevisually compared and Composition 2 (HH10) treated wounds are startingto appear similar to uninjured skin in terms of collagen arrangement,restoration of dermal appendages and epidermal structure at day 28. Thismay have implications for conditions where hair restoration would beadvantageous.

Although the foregoing discussion touches on many particular aspects andfeatures of the disclosure, the scope of the exclusive rights should notbe limited to particular embodiments disclosed herein, but insteadshould be measured by the full, lawful, valid scope of the claims thatfollow.

1. An extended release biocompatible composition for preventing orreducing scarring of an incision or wound site in a subject, comprising:a biodegradable support scaffold; and IL-10, wherein the amount of IL-10in the composition is from about 0.2 μM to about 2.5 μM.
 2. An extendedrelease biocompatible composition for preventing or reducing scarring ofan incision or wound in a subject, comprising: a biodegradable supportscaffold; and IL-10, wherein the biodegradable support scaffold isconfigured to release from about 0.015 nM to about 0.015 μM of IL-10over a period of time at the incision or wound site.
 3. The compositionof claim 1, wherein the biodegradable support scaffold compriseshyaluronan or a hyaluronan moiety.
 4. The composition of claim 3,wherein the hyaluronan is hyaluronic acid.
 5. The composition of claim1, wherein the biodegradable support scaffold comprises a heparin orheparan sulfate.
 6. The composition of claim 1, wherein thebiodegradable support scaffold comprises collagen.
 7. The composition ofclaim 6, wherein the collagen is human collagen.
 8. The composition ofclaim 7, wherein the collagen is Type-I collagen.
 9. (canceled) 10.(canceled)
 11. The composition of claim 1, wherein the biodegradablesupport scaffold comprises PEG or a PEG moiety.
 12. (canceled) 13.(canceled)
 14. (canceled)
 15. A method for preventing or reducingscarring or process characterized by fibroplasia by administering atherapeutically effective amount of IL-10 to a location in a subject fora period of time sufficient to prevent or reduce scarring or fibrosis,said administering comprising administration of the composition of claim1 to a site at risk for fibroplasia in the subject.
 16. A method forpreventing or reducing scarring or fibrosis of a site at risk forfibroplasia comprising administering a therapeutically effective amountof IL-10 to a location in a subject for a period of time sufficient toprevent or reduce scarring or fibrosis, said administering comprisingadministration of the composition of claim 1 to a site at risk forfibroplasia in the subject.
 17. A method for preventing or reducingscarring or fibrosis of a site at risk for fibroplasia in a subject,comprising: providing the composition of claim 1; and introducing thecomposition to a location at risk for fibroplasia by administration ofthe composition; and maintaining an amount of IL-10 for a period of timesufficient to prevent or reduce scarring or fibrosis at the location.18. (canceled)
 19. The method of claim 15, wherein the administration isa single administration of the composition.
 20. (canceled) 21.(canceled)
 22. The composition or method of claim 15, wherein the periodof time is at least about 3 days.
 23. The composition or method of claim22, wherein the period of time is at least about 4 days.
 24. (canceled)25. The composition or method of claim 15, wherein the period of time isabout 3 to about 7 days.
 26. The composition or method of claim 15,wherein the amount of IL-10 is from about 0.002 μM to 0.015 μM for thefirst three days and between 0.015 nM to about 0.2 nM for up to sevendays.
 27. The composition of claim 1, wherein the amount of IL-10 in thecomposition is from about 0.017 μM to about 0.035 μM.
 28. (canceled) 29.The method of claim 16, wherein the site includes a dermal layer orepidermis or other relevant anatomical site for increased fibrosis. 30.(canceled)
 31. (canceled)
 32. (canceled)
 33. (canceled)
 34. (canceled)35. (canceled)
 36. A kit comprising: an extended release biocompatiblecomposition of claim 1; and a dressing. 37-49. (canceled)